IQVIA

Solutions Engineers provide end-to-end IMOS Physician Level Data reporting support for platform clients. They work closely with various teams to understand client needs and evolve IQVIA’s platform solutions. | Candidates should have a Bachelor’s Degree and 2-5 years of relevant experience. Proficiency in SQL and the ability to manage multiple clients and projects are essential. | The Solutions Engineer (SE) Team within the IQVIA Digital Data Management organization supports the Media Operating System (OS) platform. Solutions Engineers provide end-to-end IMOS Physician Level Data (PLD) reporting support for platform clients. Working side-by-side with data, product, engineering, and client services, this team has tremendous autonomy to tackle user problems/needs and help drive the business to success every day. Together we build innovative commercial products and technical solutions through collaboration, empathy, and a readiness to challenge the status quo. Ideal candidates are consultative, analytical, technically minded, and passionate about driving results. About the Job: Own key areas of IQVIA’s analytics and reporting infrastructure Work closely with our Client Services team to understand client landscape and scale offerings for key accounts Cultivate a deep understanding of our client reporting, audience segmentation, and data needs Act as a subject matter expert (SME) during client meetings to gauge new requests and help guide key accounts through IQVIA’s unique capabilities and data solutions Work directly with Sales and Product to evolve IQVIA’s platform solutions to meet our client needs Understand the feasibility, methodology, and structural components of all areas of IQVIA’s platform and reporting capabilities Qualifications: Bachelor’s Degree 2-5 years of relevant experience Ability to prioritize workload and self-manage across multiple clients, projects, and teams Proficiency in scoping, breaking down, and building out technical requests into business solutions Experience in supporting client facing technical scoping, planning, and implementation Advanced knowledge of SQL, ability to analyze data of any kind and identify/resolve issues Ability to work with complex datasets and a familiarity with ETL processes Ability to learn our technology: Alteryx, Google Cloud Storage, BigQuery, File Transfer Protocols (FTP/sFTP), DBeaver, SQL Server, Jira, Confluence Preferred: Knowledge of digital media buying and/or hands-on experience with digital media reporting Healthcare industry knowledge across payer, provider, pharma, digital health Knowledge of pharma media measurement and reporting landscape IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $53,700.00 - $134,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

Provide education and training to nurses and physicians on medical devices during regional and national assignments without bedside care. | Must have RN degree with active license, 2+ years recent critical care nursing experience, hemodynamics knowledge, and ability to travel. | We welcome you to apply if interested! You will be asked to create an account, which takes less than one minute and requires only a username and password. The entire application takes no more than 5-7 minutes to complete. Job Description: Our RN Clinical Educators experience a unique opportunity to employ their clinical nursing expertise in a new way outside patient care, while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology. You will be responsible for training and educating Registered Nurses and Physicians on Patient and Hemodynamic monitors. • Your primary focus will be in-servicing and education only; no sales responsibilities, and no bedside care. • Per-diem position requiring travel and flexibility to work with your current schedule. • Average 1-2 assignments per month, ranging 3-5 days per assignment. Travel regionally and nationally to support customer needs. This role is a great opportunity if you have a desire to expand your talents in clinical education IQVIA takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Responsibilities: • Provide peer-to-peer education and in-servicing to nurses, physicians, and hospital staff to support medical device implementations • Assess customer-specific education needs and collaborate with staff to deliver a positive educational experience • Utilize clinical nursing expertise to answer questions and address concerns with the medical device • Provide updates, reports, and valuable feedback to client during and after in-service assignments Job Requirements: • RN Degree - Associates required, Bachelor's preferred • Active and Unrestricted RN license required • 2+ years experience in critical care (ICU or ER), in a hospital setting within the last 2 yearsrequired • Experience with hemodynamics and using pressure lines required • Ability to travel locally, regionally, and nationally required • Must be comfortable with basic software programs • Duties may require compliance with client requirements that all those performing services on-site be fully vaccinated Preferred experience: • Leadership experience (manager, educator, preceptor) can be helpful but is not required You will have a flexible schedule, an opportunity to travel, grow and expand into new opportunities while earning supplemental income and learning the medical device industry. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more athttps://jobs.iqvia.com We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.https://jobs.iqvia.com/eoe As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status.https://jobs.iqvia.com/covid-19-vaccine-status #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $40 - $45 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Provide education and training to nurses and physicians on medical devices during regional and national travel assignments. | Active RN license, 2+ years critical care nursing experience within last 2 years, hemodynamics knowledge, and travel flexibility. | We welcome you to apply if interested! You will be asked to create an account, which takes less than one minute and requires only a username and password. The entire application takes no more than 5-7 minutes to complete. Job Description: Our RN Clinical Educators experience a unique opportunity to employ their clinical nursing expertise in a new way outside patient care, while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology. You will be responsible for training and educating Registered Nurses and Physicians on Patient and Hemodynamic monitors. • Your primary focus will be in-servicing and education only; no sales responsibilities, and no bedside care. • Per-diem position requiring travel and flexibility to work with your current schedule. • Average 1-2 assignments per month, ranging 3-5 days per assignment. Travel regionally and nationally to support customer needs. This role is a great opportunity if you have a desire to expand your talents in clinical education IQVIA takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Responsibilities: • Provide peer-to-peer education and in-servicing to nurses, physicians, and hospital staff to support medical device implementations • Assess customer-specific education needs and collaborate with staff to deliver a positive educational experience • Utilize clinical nursing expertise to answer questions and address concerns with the medical device • Provide updates, reports, and valuable feedback to client during and after in-service assignments Job Requirements: • RN Degree - Associates required, Bachelor's preferred • Active and Unrestricted RN license required • 2+ years experience in critical care (ICU or ER), in a hospital setting within the last 2 years required • Experience with hemodynamics and using pressure lines required • Ability to travel locally, regionally, and nationally required • Must be comfortable with basic software programs • Duties may require compliance with client requirements that all those performing services on-site be fully vaccinated Preferred experience: • Leadership experience (manager, educator, preceptor) can be helpful but is not required You will have a flexible schedule, an opportunity to travel, grow and expand into new opportunities while earning supplemental income and learning the medical device industry. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $40 - $45 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manage and oversee clinical project management staff to ensure study deliverables meet quality, budget, and timeline goals while providing coaching, training, and performance management. | Bachelor's degree in life sciences or related field, 10+ years relevant experience including 3+ years leading teams, knowledge of clinical trials and regulatory requirements, strong leadership and communication skills. | Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to an assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction. Manage direct reports and teams in accordance with organization's policies and applicable regulations. Ensure direct report employees are fully trained; individual development is aligned; and in place to meet project and organizational needs. Able to attract; develop and retain talent. Essential Functions • Manage staff and provide guidance in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters.; • Work with individual staff to make sure all study management and project deliverables are completed as per the Contract, to achieve quality deliverables on time and within budget and in accordance with SOPs, policies and practices. As their first point of contact, provide effective and timely consultation/guidance to employees on issue resolution. • Coach and mentor employees around project planning, project review, risk management and problem solving to ensure global alignment of work practices across the team through the adoption and use of all process and technology tools and improvements by employees. • Obtain and provide regular feedback to employees from other project team members and key stakeholders to assist in personal and professional development. May attend project team meeting in order to support development needs. Identify skill and competency gaps at the individual level and work to craft development plans that will close the gaps. • Ensure direct reports demonstrate working knowledge of finances, baseline and change control in terms of scope, budget, schedule and risk/ issue management. • Train the Project Lead management team on processes and procedures. Ensure required trainings are completed on time. • Complete and discuss the Project Lead competency framework with each direct report. • Actively engage with the review of project performance dashboard for tracked information. Follow up with direct reports to ensure system and metrics compliance. • Review metrics and ensure required updates are made in IQVIA systems to ensure accurate and timely reporting is available to senior management • Proactively manage risks linked to resourcing, project and/or individual needs with other management and leadership team members to manage study issues and obstacles • Work with individual staff to identify any quality issues within the study and provide coaching on resolution of issues, including implementation of corrective and preventative action plans and escalation • Provide technical expertise and/or clinical project management experience to assigned staff for training and process improvement efforts • May Lead and/or actively participate in corporate initiatives act as a department cross-functional liaison and/or change agent. Provide technical expertise and project management experience. Qualifications • Bachelor's Degree Life sciences or related field Req • Requires 10 years of prior relevant experience, with minimum of 3 years leading teams. • Require broad management knowledge to lead teams, as well as the ability to influence others outside of own job area regarding policies, procedures, and goals.; • Knowledge of clinical trials - In depth knowledge, and skill in applying applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.; • Knowledge of clinical trials - Strong understanding of the Clinical Research industry and the relevant environments in which it operates. • People Management - Proven ability to manage a team and work through others in a global environment to deliver results to the appropriate quality and timeline metrics. Provides others with a clear direction; delegates work appropriately and fairly; motivates and empowers others; monitors/manages performance and provides feedback and coaching; recruits, develops and retains staff of a high caliber.; • People Management - Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues. • Collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences. • Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. • Leadership - Ability to manage competing priorities. • Leadership - Excellent customer service skills and demonstrated ability to understand customer needs, have difficult conversations with internal stakeholders and customers, and negotiate solutions. • Leadership - Good judgment and decision making skills. • Organization - Strong presentation skills. • Organization - Strong organizational and problem-solving skills. • Organization - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving. • Organization - Strong understanding of other IQVIA functions and their inter-relationship with Project Support Unit. • Communication - Excellent communication skills, including good command of English language. • Results Oriented - Demonstrated ability to deliver results to the appropriate quality and timeline metrics. • IT Skills - Strong software and computer skills, including MS Office applications. • IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $102,500.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Lead and execute custom primary market research studies, deliver strategic insights to clients, supervise junior staff, and manage projects from inception to conclusion. | 6-10 years market research experience (preferably healthcare), bachelor's degree (advanced preferred), strong analytical and communication skills, client-focused approach, proficiency in Excel and PowerPoint, and US work authorization. | To be eligible for this position, you must reside in the same country where the job is located. Senior Consultant, Custom Market Research About us: At IQVIA, we look for the very best people, and then give them meaningful work to do. We don’t simply think about careers, we think about contributions. Those who choose to work with us are joining a recognized global leader — a company uniquely positioned to help clients make the most of market opportunities and respond to challenges that affect global healthcare. We’re committed to blending industry expertise and advanced technology to deliver the most accurate perspectives and in-depth analytics on healthcare dynamics. To join IQVIA means you’ll be part of a worldwide organization where one person can make a difference, and where collaboration and innovation rule. Our people are creative and client-focused. They are among the best and brightest in the industry. And they bring a broad range of expertise to the table. Our people are analysts, statisticians, software engineers, consultants, sales leaders, marketing and product managers, and more. The key to our success is our people, whose experience, talent, commitment and diversity set the standard for the health information industry. Total Rewards: We invest in people through a range of initiatives in compensation, benefits, and learning and development, and we strive to create an environment where our employees are challenged, empowered and can flourish. The Custom Research business unit of IQVIA, formerly AlphaImpactRx, uses marketing research with physicians, patients and other allied healthcare professionals to drive strategic decision-making for our clients in the pharmaceutical and biotechnology industry. The Position: • We are seeking bright, motivated candidates for a full-time Senior Consultant position for candidates with outstanding strategic thinking, strong analytical and communication skills and the ability to thrive in a culture of achievement. • This is an opportunity to work in an organization with a unique position to provide seamless, integrated solutions with primary and secondary data. • The Senior Consultant participates actively in delivering strategic insights to our clients by leading and executing primary market research studies. Roles and Responsibilities Include: • Lead and execute custom, primary market research studies from inception to conclusion • Work closely with senior management to select appropriate research methodologies, design research, conduct insightful analysis, and deliver strategic insights • Act as a thought partner to clients, in collaboration with the Supervisor. • Deliver timely, error-free and high-quality projects. • Supervise a more junior project team and manage other partners on projects. • Contribute to the success of the department by developing junior staff and participating in/leading internal projects. Please Apply If You: • Bachelor’s Degree required; advanced degree preferred (Master’s degree or PhD). • Minimum of 6-10 years of experience in market research, preferably within healthcare. • Expertise in Excel and PowerPoint required. • Have the right to work in the US without Company sponsorship • Has a client-focused, consultative approach for project management --- not just an order taker, but is able to suggest alternate approaches and provide strategic insights that meet client needs. • Demonstrates a strong command of a variety of analytical and market research techniques. • Grasps key issues quickly, understands the "big picture", and links market research insights to larger business issues relevant to client needs. • Demonstrates excellent written and verbal communication skills and is effective in a variety of presentation settings. • Ability to learn quickly and work independently with minimum guidance • Ability to exercise judgment and work in a fast-paced environment • Has a strong commitment to quality. • Has a proven track record of meeting or exceeding target goals. • Has the desire to develop and mentor junior staff. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $95,300.00 - $237,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Provide administrative support for patient and site engagement initiatives in clinical trials, managing budgets, timelines, compliance, and stakeholder communications. | BA/BS degree and minimum 3 years experience in global patient recruitment and clinical trial execution with strong project management skills and knowledge of clinical trial operations. | Overview: Patient & Site Engagement (PSE) Operations Specialist (OS) services provide the PSE Managers with administrative support for the management, execution and timely delivery of tactics for patient and site-facing initiatives in support of a clinical trial. Interface with key Delivery Unit customers Trial Delivery Leaders (TDLs), Trial Delivery Managers (TDMs). Interface with key Global Clinical Operations (GCO) customers Local Trial Manager (LTM) and Site Manager (SM), suppliers, and other stakeholders involved in the development, management, and dissemination of patient and site-facing tactics. Responsibilities: • Services rendered will adhere to applicable sponsor SOPs, WIs, policies, local regulatory requirements, etc. • Comply with relevant time reporting systems, training requirements and developing therapeutic knowledge enough for role and responsibilities. • Ensure accuracy and oversight of Scope of Work (SOW) to reflect all External Service Providers planned services and budgets. This includes forecasting and proactive management of PSE trial budgets and Purchase Orders. • Keep the project plan updated in relation to timelines and budget based on the scope of work for delivery of the tools and tactics for a clinical trial. • Drive execution of tactics and initiatives through management of service providers as required by business including: creative and content development, global translations, material production, technical development of apps, websites, and other technological tools to promote patient/caregiver and/or site engagement. • Ensure compliance with sponsor policies by way of documenting Compliance review and approval of tools and tactics; maintain oversight for IRB/EC approvals, as needed. • Ensure clear communications with all stakeholders throughout the process to ensure clearly defined expectations. Stakeholders include service providers, study and clinical teams, PSE team members, leadership, and compliance. Contribute to study meetings via facilitation, attending, and/or presenting at various meetings. • Maintain deep understanding and use of sponsor finance and contracting systems. • Support the coordination of congress / conference preparations and on-site logistics, as applicable • Ensure development and delivery of presentations and workshop content at Global Investigator Meetings, Ad Hoc face-to-face meetings, and other similar meetings as needed Education and Experience Requirements: • BA/BS or equivalent, preferably in a scientific or health-related discipline. • Minimum of 3 years relevant experience in global patient recruitment and clinical trial execution with a pharmaceutical company, CRO, and/or healthcare facility/research site. • Strong clinical project management experience preferred • Expertise in the areas of drug development, clinical trial operations, and strategic planning. • Previous experience in clinical trial operations including the execution of study outreach, patient compliance and support programs. • Strong planning and tracking skills, customer focused, well organized, detail oriented and capable of successfully managing multiple projects. • Excellent time, priority, and self-management skills. Strong project management skills. • Strong team orientation: demonstrates initiative to solve problems and improve efficiency and/or customer service. • High degree of proficiency in Microsoft Excel, PowerPoint and Word. Microsoft Project. • Good written and oral communication skills. • Strong understanding of appropriate software and company systems. • Periodic travel as required IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $62,800.00 - $157,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Provide remote technical support for Optos retinal scanning devices, troubleshoot software and network issues, and assist customers and field employees. | High school diploma, 1+ year technical support experience, customer care background, knowledge of Windows OS, PC hardware, networking, and reliable high-speed internet. | Tier 2, Technical Support Representative Mon - Fri 10am - 7pm ET Contract Remote Role – Location (Open to Remote US) As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product’s value to payers, physicians, and patients. A significant part of our business is providing patient support programs on the behalf of our customers. With the right experience, you can help provide support to patients in need of available therapies. IQVIA has the world’s largest Commercial Sales & Medical Solutions (CSMS) organization dedicated to the launch and marketing of pharmaceutical and medical products. With a focus on providing talent for patient support, field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs. We are excited to announce that currently we are looking for a 100% remote (work from home—WFH) contract Technical Support Representative – Optos to join our team. In this position, you will provide telephone support of the Optos retinal scanning medical device, various Windows Operation Systems, e-mail, dialup access, and network support for customers and field employees. The Technical Support Representative – Optos will also support PC configuration and internal IT inquiries. This role will be a contract role with IQVIA managed by an external agency, with the opportunity to be converted to an IQVIA full-time employee. Job Responsibilities: • Manage and respond to customer inquiries concerning operation and configuration of the Optos Panoramic200™. • Trouble-shoot network problems including connectivity, wireless LAN access, VPN/broadband, and non-reporting issues. • Log interactions into the CRM system. • Evaluate and escalate calls to field teams for critical issues and hardware issues. • Remotely install/troubleshoot software and upgrades, data base repair, and remove of software viruses. • Research technical and software issues to identify trends for early detection and repair. • Perform data migration on customer computers. • Ability to work 40 hours per week (available shift is 10am EST – 7pm EST), including one Saturday shift (8am EST – 5pm EST) every four weeks. Minimum Education & Experience: • High School diploma or equivalent • 1+ year of Technical Support experience required • Previous experience working in a customer care environment • Extensive knowledge and practical experience of Windows operating systems including Windows 98/NT/2000/XP/Vista/7, MS Office applications, and internet browsers • PC hardware and configuration skills • Intermediate IT networking knowledge • High-speed home internet connection required. IQVIA is an Equal Opportunity Employer. We cultivate a diverse corporate culture across the 100+ countries where we operate, celebrating and rewarding teamwork and inclusiveness. By embracing our differences, we create innovative solutions that are good for IQVIA, our clients, and the advancement of healthcare everywhere. This role will be a contract role with IQVIA managed by an external agency, with the opportunity to be converted to an IQVIA full-time employee. The pay range for this role is $25.00 per hour. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manage and support nonconformance and CAPA processes including root cause investigations, compliance monitoring, and liaison duties within clinical research quality assurance. | Bachelor's degree or 6-8 years relevant experience, 6+ years pharmaceutical industry experience including 3-4 years GxP clinical research or quality assurance, strong knowledge of drug development and quality processes. | Responsibilities: • Services rendered will adhere to applicable SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc. • Main responsibilities will include, but are not limited to: • Act as process and system SME for the nonconformance and CAPA process and business/system requirements • Assist the Investigation Owner (IO) in the application of structured problem‐solving methodologies in Root Cause Analysis (RCA) investigations (Fishbone, 5 Whys, etc) independently or in support of the Root Cause Investigation team • Coach the Investigation Owner in understanding their end-to-end accountability of the entire CAPA process • Develop and maintain proficiency in the TrackWise ETS QEM system • Work with the organization to identify resources to support RCA investigations and resulting actions • Provide assistance to the record owner to ensure process requirements are met • Monitor nonconformance and CAPA deliverables / timelines for functional area by running reports, communicating upcoming deadlines to record owners and escalating concerns to management as appropriate to actively drive compliance • Act as a liaison between the record owner and the quality leader; the record owner and the Root Cause Analysis group; the record owner and the TrackWise central entry team. • Escalate any issues, as needed, to the BRQC CAPA Review Board • Raise any process or system questions or concerns to the CAPA Champions Community of Practice • Manage requests for assistance from the TrackWise central data entry team on behalf of the IO Education and Experience Requirements/Qualifications: • A minimum of a Bachelor’s degree in Science (BSc) or Arts (BA), or 6–8 years of relevant experience is required. • At least 6 years of experience in the pharmaceutical industry, with 3–4 years of GxP experience in clinical research, development, or quality assurance. • Experience in Quality Control and Compliance, Quality Assurance, CAPA processes, and/or Root Cause Analysis. • Knowledge of the overall drug development process. • Strong understanding of business processes and practices, including SOPs governing clinical research activities. • Experience in quality assurance activities, such as audits of clinical investigative sites, systems and vendors, and audits of regulatory submissions. • Ability to translate data into actionable insights and develop executable strategies. • Strong conflict resolution, negotiation, and stakeholder motivation skills. • Ability to independently plan, organize, and manage tasks. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $62,800.00 - $157,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Lead global study teams to ensure clinical studies are planned, executed, and closed on time, within budget, and compliant with regulations, managing deliverables and stakeholder relationships. | Bachelor's degree in Life Science or related field, 5+ years relevant experience including project management, knowledge of companion diagnostic studies and clinical operations, and familiarity with EU IVDR submission process. | Job Summary The Project Lead is responsible for ensuring that all studies are designed, planned, executed, monitored, closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled, while assuring compliance to all applicable regulatory requirements. Responsible for the timeline and budget planning and execution of studies. Assigns and ensures delivery of specific tasks to/from other members of the study team. Provides oversight to outside support including CROs, consultants and/or medical advisors. Responsibilities • Leading the global study team with full accountability for study deliverables regarding quality, budget, and timelines. • Developing key study documents (e.g., Design Validation Plan, protocol, study training materials, study forms and templates, study report). • Overseeing planning and operational aspects of companion diagnostics studies sponsored by Pharma partners. • Ensuring adherence to regulations, guidelines, and standard operating procedures, and ensuring audit/inspection readiness. • Executing sponsored studies for assigned areas of focus through all study phases (planning, start-up, conduct, and close-out). • Overseeing projects to ensure completion on-time, within scope, and budget; tracking project performance to analyze the completion of short and long-term goals. • Building and maintaining strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders, and other alliance partners, including CROs. • Collaborating across Clinical Operations and other functions to develop and implementing best practices across Clinical Operations. Requirements • Experience with Companion Diagnostic (CDx) studies. • Team-oriented with excellent collaboration skills with a cross-functional team. • Open-minded to learn new ways of doing things while leveraging previous experience. • Knowledge of or experience with EU In Vitro Device Regulation (IVDR) submission process • Minimum of a bachelor’s degree in Life Science and/or relevant expertise in the Healthcare Industry or a related field, at least 5years of prior relevant experience including > 1 year’s project management experience. • Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Achieve sales quotas by developing and executing sales plans, cultivating customer relationships, managing proposals and contracts, and supporting marketing activities for FSP services in clinical research. | Bachelor's degree with 12 years related experience including 5 years CRO/pharmaceutical sales experience, knowledge of clinical development and CRO operations, and experience in FSP sales and delivery. | Director, Data Sciences, Safety and Regulatory, FSP Sales will contribute to a major segment of the Sales organization – FSP services for the Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions - and will be responsible for achieving FSP Sales targets from assigned portfolio of accounts. Core responsibilities include: • Achieving annual sales quota for assigned account portfolio, including individual quotas for each line of business. • Developing relationships with both IQVIA traditional customer base and non-traditional/new customers and markets, and actively prospecting new business opportunities for FSP services. • Establishing and executing a comprehensive sales plan for each target account. Monitor actions and results against plan. • Maintaining an advanced understanding of IQVIA’s specialized FSP offerings and providing “best practice” advice and solutions throughout sales cycle. • Cultivating relationships with key decision-makers within Account Teams and developing in-depth knowledge of the customers' organizations. • Identifying and responding to customer needs, defining potential opportunities, and proposing appropriate strategy/solution to customer. • Coordinating and overseeing the development of proposals and contracts for assigned accounts. • Maintaining customer, proposal, and contract tracking for assigned portfolio of accounts. • Managing customer inquiries and requests for information from both internal and external customers in a timely manner. • Developing and maintaining knowledge bank of IQVIA's position vs competitors in the FSP market, including positioning and pricing, specific reasons for awards and non-awards, duration of contractual engagements, and status. • Maintaining general knowledge of all IQVIA R&DS services for appropriate cross-sell opportunities and working across company's service lines and with sales teams to cross-promote and respond to RFPs as well as develop internal relationships needed to create solutions designed using multiple services. • Support sales and marketing services by attending, participating, and speaking at trade shows and industry conferences. Skills and abilities: • Must have direct experience with FSP delivery models, principles, pricing, and commercial terms. • Must have a proven track record with high-level customer contacts. • Must have excellent verbal, written, and presentation skills • Must act with a sense of urgency and be able to work both independently and within a team environment. • Must be Sales-driven, knowledgeable, consultative, a problem solver, customer focused, creative, resourceful, and fast-moving. Requirements: • Bachelor's Degree • 12 years related experience, including 5 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or • Equivalent combination of education, training and experience Req • General knowledge of the Clinical Development space and Clinical Research Organization (CRO) operations are required. • Experience in the sales, contracting, and delivery of services in an FSP model. • Sales experience in a Clinical Research Organization, BPO, or Clinical Staffing Agency is required. • Operational experience in Clinical Data Management, Biostatistics, Statistical Programming, Medical Writing, Lifecycle Safety or Regulatory Affairs field is beneficial. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $111,200.00 - $309,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manage and coordinate strategic initiatives, operational excellence, and integration efforts to support US Medical Affairs and IQVIA Health Communications Group's growth and collaboration. | Bachelor's degree with 5+ years in pharmaceutical, consulting, strategy, or business operations roles, strong communication and leadership skills, and ability to manage multiple complex initiatives. | Strategic Operations Associate, US Medical Affairs & IQVIA Health Communications Group Position Purpose The Strategic Operations role provides critical operational discipline and strategic thinking to US Medical Affairs and the IQVIA Health Communications Group. This position ensures effective execution of strategic initiatives, process optimization, and day-to-day business needs, with an emphasis on enabling collaboration, clarity, and long-term growth. As IQVIA Health Communications Group rapidly evolves through continued expansion and integration, and Medical Affairs continues to serve as a strategic priority for the organization, this role will play a pivotal part in positioning these teams for sustained success. Key Responsibilities Operational Excellence • Coordinate and manage team recurring forums, including townhalls, leadership meetings, and others, ensuring clear objectives, outcomes, and follow-up • Liaise with senior leaders across IQVIA, representing the perspective and needs of US Medical Affairs and IQVIA Health Communications Group to ensure alignment and effective collaboration • Partner with enabling corporate functions (Finance, HR, Marketing) to support reporting, operational success, and remove barriers to execution • Track all key priorities and outstanding deliverables and ensure follow up IQVIA Health Communications Group Operationalization & Integration • Oversee, develop, and facilitate cross-functional workstreams that support the ongoing evolution of the agencies, including shared services, vendors and contractors, marketing, go-to-market, and other priority areas • Partner with agency leads to understand agency-specific challenges and needs, ensuring solutions are tailored and actionable while maintaining alignment with overall strategy • Support the integration of acquired agencies in partnership with the Integration Project Manager, to help guide functional and cultural transitions and ongoing alignment to IQVIA processes and values • Identify and address gaps in the integration process and facilitate a resolution • Drive awareness and visibility of IQVIA's Health Communications Group internally and externally through helping to craft messaging, materials, and communications Strategic Initiatives • Propose, lead, and support high-impact initiatives that advance the priorities of US Medical Affairs and IQVIA Health Communications Group • Partner with senior leaders to refine and implement strategic initiatives • Maintain strong communication with go-to-market teams to help them understand IQVIA Health Communications Group and Medical Affairs' unique positioning and value, ensuring alignment on strategy and opportunities • Anticipate challenges and proactively propose solutions to maintain momentum on critical initiatives • Stay attuned to the evolving market landscape across the Medical Affairs and health communications industries, bringing forward insights and implications that inform strategic planning and positioning Experience & Skills Required: • Bachelor's degree required; advanced degree preferred • 5+ years' experience in pharmaceutical, consulting, strategy, or business operations roles • Demonstrated success in strategic program management or business operations • Exceptional communication skills, with the ability to craft compelling executive-level materials (PowerPoint), facilitate cross-functional meetings, and effectively present to senior stakeholders • Ability to influence and build credibility with senior leaders across functions and geographies • Strong problem-solving and critical thinking capabilities, with ability to prioritize and manage multiple complex initiatives. • Familiarity with IQVIA operating models, financial reporting, and go-to-market structure is desirable • Ability to quickly learn and adapt in an evolving environment, demonstrating agility in supporting dynamic team and organizational needs Please Note: In order to be eligible for this remote role, you must reside within the country in which the position is posted. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $95,300.00 - $237,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manage and coordinate field action deliverables including customer remediation, scheduling, and financial reporting for medication management solutions projects. | HS diploma minimum, strong communication and customer service skills, ability to learn technical systems quickly, advanced MS Office and Salesforce skills, and ability to work remotely with flexible hours. | Our MedTech Project Coordinator will support the SDS organization within our Medication Management Solutions (MMS) Business Unit by managing field action deliverables in compliance with our quality and regulatory requirements. These deliverables include supporting customer remediation for recalls (where applicable), preparing the remediation team for new recalls, contacting customers to schedule remediation efforts, and support financial reporting for Dispensing field actions. The Project Coordinator will have solid project management skills, attention to detail as well as strong process execution and analytical skills. As part of a remote team, the Project Coordinator will be expected to set his/her own work direction and complete tasks with minimal supervision. The Project Coordinator will be responsible for managing customer remediation associated with Field Actions, as well as other small projects, as needed. What you will be doing in the role: • Plan, coordinate, and execute small project, as assigned • Manage customer remediation for all applicable field actions • Monitor and report on field action budget, both expense to date and forecast • Attain required expertise in all databases that house product data for the platform (SAP, SharePoint) • Attain a thorough knowledge of all BD processes for field actions/recalls • Assist Senior Project Managers with preparing the remediation team for new field actions • Contact customers to schedule remediation projects with the customer, including building out detailed remediation project schedules with customers. Job Requirements: • HS Diploma minimum is required or higher degree is preferred. • Excellent writing skills and the ability to communicate accurately and concisely in English • Ability to gain new technical skills quickly • Strong customer service skills and positive attitude • Ability to communicate complex technical concepts in layman’s terms • Advanced skills with Microsoft Office products and Salesforce • Ability to meet tight deadlines and handle changing priorities Travel Requirement: • This is a Remote; work from home position that requires Internet and the ability to be flexible in different time zones. The ideal candidate will be located physically on the East or West Coast working EST or PST. Preferred Attributes: • Bachelor’s Degree in Engineering, Technology, or Life Sciences preferred. • Two or more years of experience in project management, preferred • Prior experience within a regulated industry (e.g., medical device, pharma, automotive, aerospace), preferred • Managed/supported projects cross-functionally in an iterative, fast paced environment • Excellent verbal and written communication skills required • Strong analytical, problem-solving, and interpersonal skills • High attention to detail while managing multiple complex deliverables and stakeholder groups required • Ability to learn quickly, deal with ambiguity, take initiative and achieve results required IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this. • Please note: Due to the nature of this role, it is not eligible for Visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $27-$29 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manage and deliver small to medium clinical trial connected device projects ensuring quality, budget, and timeliness under supervision. | Bachelor's in life sciences or healthcare, 3 years industry experience, leadership, organizational, communication, and customer service skills. | Job Overview Manage small to medium size Connected Devices that are stand-alone or full-service in scope, across all clinical trial phases. With support from Senior Project Manager, ensure all project work is completed to the sponsor's satisfaction, on time and within budget and in accordance with policies and procedures. Essential Functions • Under supervision, plan, initiate, execute, control, and deliver projects in accordance with the Scope of Work agreed with the customer. • Lead the Connected Devices cross-functional teams to ensure successful delivery of assigned projects. • Ensure that consistent and appropriate project specific guidelines are documented and circulated to all project team members and that the team is well-trained on these guidelines. • Track project progress, identify and evaluate project risks and take advice from superiors on corrective action as appropriate. • Prepare and present project information at internal and external meetings. • With guidance, manage the project financials accurately and appropriately ensuring project goals are achieved according to customer’s expectations and within the scope of the project. Ensure revenue recognition and forecasts are calculated accurately and change orders executed where appropriate. • Conduct an ‘End of Project’ review meeting to ensure that all project activities have been completed in full. • Keep Connected Devices leadership fully informed of any project issues that may impact quality, budget, and timeliness of project delivery to the customer’s satisfaction. Request support and advice for timely issue resolution as required. • Provide input to line managers on their project team members’ performance relative to project tasks to aid career development. Qualifications • Bachelor's Degree Life science or health care related discipline • Three years industry experience • Equivalent combination of education, training and experience • Good leadership skills • Good ability to prioritize, schedule and organize • Good interpersonal and communication skills • Good problem-solving skills • Excellent customer service skills • Good Microsoft Office skills • Ability to establish and maintain effective working relationships with coworkers, managers and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $59,900.00 - $149,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Provide in-hospital support during atherectomy cases, educate physicians on clinical procedures, and maintain hospital credentialing compliance. | Must have active clinical credentials (RT, RCIS, RN, or Respiratory Therapist), associate degree, hospital experience, valid driver’s license, and ability to clear vendor credentialing. | Our MedTech Vascular Assistant experiences a unique opportunity and leverage your clinical expertise in a dynamic role that goes beyond traditional patient care. Collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology. What you will be doing in the role: • Supporting in-hospital case coverage on peripheral and/or coronary atherectomy cases. • Demonstrate a high level of understanding in these types of situations through offering education and clinical knowledge to physicians performing the case/medical procedure. • Per-diem schedule but can amount to 1- 2 days of work each week and can work with a current Part Time or Full-time • Training for this role will be provided and is paid. You will have an opportunity to travel, grow, and expand into new opportunities while earning supplemental income and learning the medical device industry. Job Requirements: • Active and unencumbered Radiology Technician (RT), RCIS, RN or Respiratory Therapist (RT) credential and licensure • Associates degree required • Hospital or industry experience required. • Ability to clear hospital vendor credentialing requirements. • Candidates must possess a valid driver’s license and will be subject to a review of their driving record prior to hire. Preferred Attributes: • Preferred unit or environment experience – Emphasis on Fluoroscopy, cardiac catheterization lab, interventional radiology, operating room, outpatient access center, ambulatory surgery center, ultrasound, or dialysis center. • Leadership experience (manager, educator, preceptor) can be helpful but is not required. • 1 year experience preferred, Bachelor’s degree preferred IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this. • Please note: Due to the nature of this role, it is not eligible for Visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is 50-55 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manage and coach inside sales representatives to achieve sales forecasts and product adoption through performance monitoring and training. | BA/BS degree, 3-5 years inside sales leadership in MedTech or Pharmaceutical, inside sales/remote engagement experience, coaching skills, and strong communication. | Join the IQVIA team, where diversity and inclusion thrive in a workplace committed to improving patients' lives. We recognize that our employees are crucial to our mission's success and have been acknowledged as a fantastic workplace. At IQVIA, we provide benefits and programs to empower you to develop and advance in your career. We are particularly interested in attracting individuals with drive and initiative, individuals who are ready to propel their careers forward and contribute to driving performance. As a global leader in commercial solutions, IQVIA is dedicated to delivering impact both nationally and internationally. Our collaborative teams play a vital role in ensuring that biopharmaceuticals, medical devices, and patient support services reach those who need them. We offer valuable insights to customers and demonstrate product value to payers, physicians, and patients. Whether acting as a sales force to physicians or providing education to patients or prescribers, you can contribute to delivering real-world medical breakthroughs with the right experience. Explore the possibilities and be part of shaping a healthier future with us. We are excited to announce that in partnership with our client Ethicon, a global leader in the medical device space, we are currently looking for an Inside Sales Manager to join our team. The Inside Sales Manager is primarily responsible for achieving sales forecasts and gaining adoption and utilization of the product portfolio through the development of Inside Sales Representatives by coaching and providing guidance in territory management and communications. Responsibilities • Development and coaching of Inside Sales Representatives • Handle performance reviews, personnel issues, discipline and termination of Inside Sales Representatives • Inside Sales Manager shall monitor calls: to develop and motivate Inside Sales Representatives for the attainment of sales objectives; to assess and monitor activity and work schedules; to monitor and manage reporting by Inside Sales Representatives, including call reporting, and sample reporting (when applicable) • Communicate with Client and Project Lead on regular and timely basis • Advance listening and decision-making skills • Ability to understand and convey complex product-related information in an educated, reassuring, and professional manner while in a real-time environment • Ability to provide coaching and feedback to improve individual performance of the Inside Sales Representative team. • Ability to be flexible as needed to meet the fluctuating business needs • Set Clear measurables for the team with weekly engagement with leadership • Enhance Training Programs: Focused on product knowledge and sales techniques. • Monitor Progress: Regular check-ins and KPIs tracking to ensure alignment and agility. • Foster Collaboration: Encourage cross-team communication and sharing of best practices Required Qualifications: • BA/BS degree required • Minimum 3 to 5 years inside sales leadership experience in MedTech, Pharmaceutical or B2B required • Inside sales/remote engagement experience required • Experience developing and coaching high performing inside sales teams • Experience maintaining accurate records of all sales activities • Proven ability to consistently meet/exceed defined sales goals • Exceptional verbal and written communication skills, action oriented, driven for results, adaptability #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $80,000-$90,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Lead preparation and review of medical writing documents, manage project timelines and budgets, mentor junior staff, and communicate with clients. | Bachelor's degree in life sciences required, 5+ years of relevant medical writing experience, strong knowledge of clinical study documentation, statistics, and regulatory standards. | Aperçu du poste : Agit à titre de rédacteur médical principal pour la plupart des types de projets de rédaction. Prépare les documents attribués conformément aux procédures opérationnelles normalisées (PON) d’IQVIA, aux exigences du client ainsi qu’aux échéanciers convenus. Effectue la révision principale des livrables de rédaction médicale standards. Établit les échéanciers et discute/répond aux commentaires du client. Fournit une rétroaction écrite et verbale au personnel subalterne, ainsi qu’aux clients lorsque cela est approprié. Se tient à jour des connaissances actuelles en rédaction médicale et/ou technique ainsi qu’en réglementation, y compris les Bonnes pratiques cliniques (BPC), de même que des avancées et développements dans le domaine de la mise au point de médicaments et de la rédaction médicale et/ou technique. Fonctions principales : • Assume un rôle de premier plan dans la préparation des documents assignés, notamment en confirmant la portée de la tâche, les gabarits et les spécifications, en négociant et respectant les échéanciers, en organisant les révisions de documents et en communiquant directement avec le client. • Planifie et organise la charge de travail pour les projets et tâches attribués : identifie les besoins du projet, suit les échéanciers et met en œuvre les demandes du client. • Dirige de façon autonome des réunions portant sur des sujets plus complexes. • Peut présenter les processus standards de rédaction médicale lors de réunions de présentation dans le cadre d’un appel d’offres. • Participe à la formation et au développement du personnel subalterne, soit de manière formelle en tant que mentor attitré, soit de façon ponctuelle auprès de collègues locaux ou d’autres membres de l’équipe. Peut concevoir et offrir une formation à l’équipe mondiale sur un sujet dans lequel il ou elle possède une expertise particulière. Peut contribuer à l’élaboration de présentations sur la rédaction médicale et les présenter à d’autres équipes d’IQVIA. • Peut agir à titre de gestionnaire de projet pour un projet de rédaction médicale plus complexe, mais unique, incluant des responsabilités liées aux finances du projet et à la facturation. • Effectue les activités financières liées au projet, y compris le suivi et la prévision des heures estimées. • Propose, révise et approuve les budgets et les estimations de coûts pour les projets courants, y compris l’estimation des heures nécessaires aux tâches de rédaction médicale. • Peut assumer un rôle de responsable client à petite échelle ou assister un responsable de partenariat déjà en place dans ses fonctions. • Peut représenter sa région ou son centre dans le cadre d’une initiative en rédaction médicale ou d’une initiative interfonctionnelle. • Encadre et participe activement à l’élaboration d’idées novatrices. Peut représenter l’équipe de rédaction médicale lors d’un audit général des capacités. Qualifications : • Baccalauréat en sciences de la vie ou dans un domaine connexe requis • Maîtrise en sciences de la vie ou dans un domaine connexe souhaitée • Doctorat en sciences de la vie ou dans un domaine connexe souhaité • Nécessite généralement au moins 5 ans d’expérience hautement pertinente et des niveaux de compétence connexes. • Connaissance approfondie des exigences structurelles et de contenu des rapports d’étude clinique, des protocoles et de documents similaires, ainsi que capacité à repérer les lacunes, erreurs et incohérences dans un protocole ou un rapport. • Bonne compréhension des méthodes statistiques couramment utilisées dans les essais cliniques et/ou de l’interprétation de leurs résultats. • Capacité à réviser efficacement un plan d’analyse statistique et à repérer les lacunes, erreurs et incohérences dans les résultats statistiques. • Capacité à intégrer, interpréter et résumer des données provenant de diverses sources de manière claire et concise. • Expérience significative à titre de rédacteur principal dans la préparation de rapports d’étude clinique (REC) et de protocoles, avec des rétroactions constamment positives de la part des clients et des collègues. • Connaissance approfondie du développement de médicaments, de la rédaction médicale et de la réglementation connexe. Bonne compréhension des principes statistiques et de la terminologie médicale dans un large éventail de domaines thérapeutiques. • Excellentes compétences en communication écrite et orale, y compris en rédaction grammaticale et technique. • Excellente attention aux détails et à la précision. • Excellente maîtrise de la communication et de la négociation auprès des clients et des gestionnaires de projet. • Capable de transmettre des messages délicats de manière constructive. • Fait preuve d’initiative et de bon jugement face à des situations ou des défis nouveaux liés à un projet ou à un document. • Aptitudes démontrées pour le travail collaboratif et la réflexion autonome. • Fait preuve d’assurance et de maturité dans la plupart des situations courantes de rédaction médicale. • Fait preuve de bon jugement en demandant l’avis du personnel de niveau supérieur. • Capacité à établir et à entretenir des relations de travail efficaces avec les collègues, les gestionnaires et les clients. • Capacité à gérer efficacement plusieurs tâches et projets. • Capacité à évaluer de manière proactive les risques et les problèmes potentiels, à rechercher des solutions et à en discuter de façon appropriée avec les collègues et les clients. • Doit avoir une bonne maîtrise des outils informatiques. Job Overview: Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments. Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. Essential Functions: • Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer. • Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests. • Lead meetings on more challenging topics independently. • May present on standard Medical Writing processes at full-service bid defense meetings. • Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups. • May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities. • Complete project finance activities, including monitoring and forecasting budgeted hours. • Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks. • May take on a small customer lead role or assist an established partnership lead in their role. • May represent region or site on a Medical Writing initiative or cross-functional initiative. • Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit. Qualifications: • Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Required • Master's Degree Master's Degree in life sciences related discipline or related field Preferred • Ph.D. Ph.D. in life sciences related discipline or related field Preferred • Typically requires at least 5 years of highly relevant experience and related competency levels. • In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report. • Good understanding of common statistical methods used in clinical trials and/or interpretation of their results. • Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output • Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner. • Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues. • In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas. • Excellent written and oral communication skills including grammatical/technical writing skills. • Excellent attention to detail and accuracy. • Confident and effective communication and negotiation skills with customers and project managers. • Able to deliver difficult messages in constructive manner. • Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges. • Demonstrated abilities in collaboration with others and independent thought. • Demonstrates confidence and maturity in most routine medical writing situations. • Demonstrates good judgement in requesting input from senior staff. • Ability to establish and maintain effective working relationships with coworkers, managers and customers. • Ability to effectively manage multiple tasks and projects. • Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers. • Must be computer literate IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $84,400.00 - $211,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Educate hospital pharmacy staff on a medical device, provide customer support, and deliver feedback during in-service assignments. | Active Pharmacy Technician license, hospital and oncology experience preferred, ability to travel and meet hospital credentialing requirements. | Our MedTech Clinical Educator with a focus on Pharmacy Technician role experience a unique opportunity to employ their technician expertise in a new way, while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology. You will be responsible for educating end users on a new product in hospital pharmacy facilities. The product being supported is a closed system drug transfer device used in an oncology setting. Our ideal candidate will enjoy educating others, presenting to groups, and have a professional business acumen including strong communication and soft skills. This is a great opportunity to continue making an impact in healthcare while exploring medical device education. You will have a flexible schedule, an opportunity to travel, grow and expand into new opportunities while earning supplemental income and learning the medical device industry. What you will be doing in the role: • Utilize Pharmacy Technician expertise to answer questions and address concerns with the medical device • Assess customer-specific education needs and collaborate with staff to deliver a positive educational experience • Provide updates, reports, and valuable feedback to client during and after in-service assignments You will have an opportunity to travel, grow, and expand into new opportunities while earning supplemental income and learning the medical device industry. Job Requirements: • Active and current Pharmacy Technician license • Must be available at least two weeks per month for assignments • Ability to stand for long periods of time, bend, kneeling and some lifting of equipment may be required of up to 50 pounds • Ability to clear hospital vendor credentialing requirements, including providing proof of up-to-date vaccination status, required Travel Requirement: • Full-time commitment with travel flexibility. • This is a per-diem position, requiring travel regionally and nationally to support customer needs while having the flexibility to work with your current schedule. On average there are 1-2 assignments per month, ranging from 3-5 days long per assignment. • Driving is considered a business requirement for this role. Candidates must possess a valid driver’s license and will be subject to a review of their driving record prior to hire. • Personal vehicle required for job-related assignments up to 3 hours from home. • Located within 1 hour of a major airport. • Travel, and your time traveling is paid. Preferred Attributes: • 2- 3 years minimum hospital experience preferred • 1 year or more of Oncology experience highly preferred • Leadership experience preferred IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this. • Please note: Due to the nature of this role, it is not eligible for Visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $30 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Provide nursing education and support to healthcare providers and patients about a Parkinson's Disease product through presentations and workshops. | Requires RN license, 3-5 years nursing experience with Parkinson's or GI/endoscopy, clinical teaching experience, and willingness to travel extensively. | External Job Description We are excited to announce that at this time we are looking for Nurse Educators to join our team of over 10,000 global field representatives in several regions making over 20 million product details annually for our pharmaceutical and biotech clients. Clinical Educators: This is a full time, field based position. Our Clinical Educators interact with health care professionals to improve treatment adoption in a variety of disease states that are frequently under-diagnosed, misdiagnosed, or under-treated. The Clinical Educator will provide nursing instruction services to Health Care providers to deliver educational programs regarding a Parkinson's Disease product. The Educator will also provide educational support to patients with Parkinson's Disease regarding the product. The Educator will educate practices through presentations and workshops. Qualifications/Experience 4 year Bachelor's degree required, RN required Advanced Practice Nurse preferred (NP or Masters) Minimum 3-5 years experience with Parkinson's or GI/endoscopy experience preferred Current nursing license in good standing Clinical training/teaching experience recommended Endoscopy or Operating room experience desirable Pharmaceutical Or Medical Device Experience Required. Understanding of regulatory environment and compliance obligations Willing to travel extensively (90%) Competencies Very strong time management skills Strong planning and prioritization skills Strong and effective presentation skills; excellent communications skills – both written and verbal Ability to work and drive for results in cross-functional teams Drive and enthusiasm Exceptional interpersonal skills Fully competent in MS Office (Word, Excel, PowerPoint) IQVIA offers a friendly, progressive work atmosphere and a comprehensive benefits package including medical, dental, life insurance and vision coverage, tuition assistance, bonus plan and 401(k). We look forward to the prospect of working with you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $110,000 - $125,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Promote endocrinology/diabetes products by phone to healthcare professionals, achieve sales forecasts, and coordinate sales strategies. | Requires a 4-year degree, minimum 2 years BTB sales, 1 year inside sales, with pharmaceutical or medical device experience preferred. | As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product’s value to payers, physicians and patients. A significant part of our business is acting as the company’s sales force to physicians or providing nurses to educate prescribers. With the right experience, you can help deliver medical breakthroughs in the real world. IQVIA has the world’s largest Commercial Sales & Medical Solutions (CSMS) organization dedicated to the launch and marketing of pharmaceutical and medical products. With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs. We are excited to announce that in partnership with a global leader in diabetes care, we are currently looking for Inside Pharmaceutical Sales Representatives to join our team. In this position, you will promote products in the Endocrinology/Diabetes space. The Inside Pharmaceutical Sales Representative is primarily responsible for achieving sales forecast and gaining adoption and utilization of the product portfolio. This is accomplished by establishing mutually beneficial business relationships with targeted accounts and physicians key to the sales success of the promoted products. The sales representative is also responsible for coordinating sales strategies with appropriate teammates to maximize sales in assigned territory. Responsibilities • Ability to deliver accurate product information, feature/benefits and recommended utilization to Healthcare Professionals by phone • Advance listening and decision-making skills • Ability to understand and convey complex product-related information in an educated, reassuring, and professional manner while in a real-time environment • Ability to accept and quickly apply coaching and feedback to improve individual performance and customer experience • Ability to handle multiple tasks such as actively listening to our caller’s need while navigating our CRM and consistently providing accurate and complete information on the requested topic. • High work ethic, reliable and punctual in reporting for scheduled work • Ability to be flexible as needed to meet the fluctuating business needs Required Qualifications: • 4-year degree from an accredited college or university • Minimum 2 years of business to business (BTB) sales experience required • Minimum 1 year of inside sales experience required • Pharmaceutical or Medical Device Experience preferred • Endocrinology/Diabetes experience preferred • Exceptional verbal and written communication skills • Successful candidates will demonstrate the following competencies: Action Oriented, Drive for Results, Sales Persuasion, Dedication, Perseverance, Ingenuity, and Adaptability Preferred Qualifications: • All the Required Qualifications, plus: • Related experience in the Endocrinology/Diabetes space • Demonstrated ability to manage and develop an assigned territory via inside sales CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $30-$33 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Provide patient-centered education and support for prescribed therapies through multiple communication channels to promote treatment adherence. | Active RN license with 5+ years clinical experience, nursing degree preferred, strong communication and time management skills, and willingness to travel extensively. | As a global leader in commercial solutions, IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to their markets, helping them demonstrate the value of their products to payers, physicians, and patients alike. A core part of our mission includes serving as the sales force for biopharma or providing nurse educators who support patients and prescribers. With the right experience, you can help bring medical innovations to life in real-world settings. We’re excited to announce an opportunity to join our team of over 10,000 field professionals worldwide—we’re currently hiring a Nurse Educator to support our pharmaceutical and biotech clients. Nurse Educator At the heart of our business strategies is a commitment to patients. The Nurse Educator Program is a patient-centered, educational initiative designed to support individuals living with chronic conditions who have been prescribed specific therapies. Nurse Educators play a vital role in helping patients understand their treatment, manage their condition, and access relevant resources related to their prescribed medication. This role involves one-on-one engagement with patients through various channels, including in-person visits, phone calls, video conferencing, email, and SMS—always in strict alignment with program guidelines. Please note: this is an educational role only. Nurse Educators do not provide clinical care or medical advice. Role Overview: Nurse Educator As a Nurse Educator, you will play a key role in supporting patients by connecting them with program-approved resources and delivering personalized education on chronic disease management and prescribed therapies. This role is designed to empower patients, promote treatment adherence, and encourage meaningful dialogue with healthcare providers. Key Responsibilities • Facilitate connections between patients and approved educational resources. • Deliver direct, disease-specific education and training related to prescribed medications. • Support multiple disease states and therapies as needed. • Promote behavioral change through patient-centered education to improve treatment adherence. • Encourage effective communication between patients and their healthcare providers. Qualifications • Bachelor’s degree and/or BSN preferred. • Active RN license in state of residence; compact multi-state license preferred where applicable. • Nursing license must be current and in good standing. • Minimum of 5 years of clinical experience in healthcare (hospital, home health, pharmaceutical, or biotech settings). • Prior experience as a nurse educator is preferred. • Bilingual in English and Spanish is a plus. • Valid driver’s license required. • Must reside within the designated territory. • Experience in direct patient interaction with a focus on adherence and persistence. • Strong understanding of clinical data and pharmacology. • Excellent time management, planning, and multitasking skills. • Effective presentation and motivational skills; strong interpersonal and communication abilities. • Ability to work independently and cross-functionally. • Dedicated home workspace required. • Adaptability to changing responsibilities and environments. • Proficiency in Microsoft Office (Word, Excel, PowerPoint) and iPad technology. • Flexibility to work evenings and weekends as needed. • Willingness to travel up to 60–70%. • Compliance with client vaccination requirements may be necessary. Compensation • Competitive annual salary • Car allowance • Bonus eligibility IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role is $95,000-$100,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.