TriNetX LLC

Conduct data analyses using EHR and claims data, implement study protocols, support client-facing RWE studies, and contribute to scientific publications. | Advanced degree in health or quantitative discipline, proficiency in SAS and SQL, experience with real-world data and observational studies, strong communication and organizational skills. | POSITION TITLE: Research Analyst LOCATION: REMOTE US This position reports to our global HQ in Cambridge, MA and is fully remote within the US. Travel is expected when needed. TriNetX is a remote-friendly company but is currently only registered for employment in certain states. To be eligible for employment, you must reside in one of the following states: AZ, CA, CO, CT, DE, FL, GA, ID, IL, KY, MA, MD, ME, MI, MN, MO, MT, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TX, UT, VA, VT, WA, WI Who we are: TriNetX was founded on the idea that incorporating real-world data (RWD) results in better clinical trial design and improves site selection and patient recruitment process. In addition, fit-for-purpose RWD with proper study design and robust analysis would generate relevant real-world evidence (RWE) to advance the collective understanding of human health and support regulatory decisions of medical products. TriNetX has a worldwide presence, with a global headquarter located in Cambridge, Massachusetts, EU headquarter in Ghent, Belgium, and additional offices in London, Madrid, Melbourne, Sao Paulo, Singapore, Tokyo, Germany, and Santa Rosa, California. TriNetX is one of the fastest-growing, privately held companies in the area's life sciences corridor. What challenges we work on: TriNetX is the global health research network that optimizes clinical research and generates actionable RWE. TriNetX combines real-time access to electronic health record (EHR) data with state-of-the-art study design and analytics to answer complex research questions. Each member of our community shares in the consolidated value of our global, federated health research network that contributes to health care improvement. Our Insights and Evidence Generation (IEG) Team is led by internationally recognized experts in RWD and RWE. We generate insights and evidence around disease progression, treatment patterns, and disease burden, and support clinical trials, labeling, safety and effectiveness studies, and reimbursement discussions. Our team has expertise in regulatory studies and provides strategic guidance around supplemental approvals, and post-marketing commitments and requirements. Who we are looking for: Our customer base, networks, and product offerings are growing rapidly, and we are expanding our Insights and Evidence Generation team with the hiring of a Research Analyst. This hire will play a key role in the organization and analysis of data from our electronic health record (EHR) databases, health insurance claims, and chart review data supporting industry-sponsored and publicly funded RWE studies and related IEG engagements. This person will work alongside Scientific and Strategic Leads to implement study protocols and ensure that methodologically, statistically, and scientifically sound deliverables are provided to our life sciences customers and other strategic collaborators. Specific activities include basic and advanced analyses of RWE data using SAS, populating study results, supporting proposal, protocol, and report development, and organizing coding libraries and other key resources. The Research Analyst will also use the TriNetX platform, data, and tools to aid in cohort identification for specific projects. The ideal candidate is someone passionate about the use of real-world data to inform drug development, approval, reimbursement, and treatment decisions across the spectrum of acute and chronic diseases and utilizing SAS analyses to answer potentially challenging research questions. What you will be doing: • Serve as the primary or validation programmer for up to 4 client-facing RWE observational studies. • Build data queries and conduct data analyses using the TriNetX Research Platform. • Program to implement data development (subject identification, inclusion and exclusion criteria) to support research projects. Carry out patient attrition, descriptive analyses, and outcomes analyses involving advanced methods. • Discuss results with research leads and client study teams. • Contribute to the development of study proposals, protocols, reports, code lists, abstracts, and manuscripts. • Support standardization of documentation and maintenance of coding programs. • Support internal research projects. • Co-author scientific papers with colleagues, collaborators, and clients. What you bring to TriNetX: • Advanced degree in a health-related or quantitative discipline strongly preferred; undergraduate degree with significant professional experience will be considered. • Working knowledge of SAS and SQL required. Experience with Databricks, Python, or R a plus. • Proficiency in Microsoft Office Excel. • Experience with real-world data (e.g., EMR, open and closed insurance claims) and implementing complex methodologies for the conduct of observational studies. • Knowledge of and experience working with medical and billing code systems. • Ability to plan, organize, and execute multiple tasks simultaneously while maintaining accuracy and attention to detail. • Excellent communication skills Learn more about TriNetX: Please feel free to check out our website www.trinetx.com and our careers page www.trinetx.com/careers/ to learn more. You can follow us on LinkedIn https://www.linkedin.com/company/trinetx, The Muse https://www.themuse.com/profiles/trinetx and be sure to read our blog https://trinetx.com/blog/ Interested in joining our community? TriNetX is an Equal Opportunity Employer. All persons are considered for employment without regard to their race, color, creed, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex or gender, marital status, sexual orientation, genetic information, gender identity, veteran status, or any other characteristic or status protected by applicable federal, state, or local laws. This Organization Participates in E-Verify This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9. E-Verify Works for Everyone For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS. 888-897-7781 https://www.e-verify.gov/

Manage and develop high-quality, on-time proposals including writing, budgeting, coordinating with commercial teams and clients, and improving internal proposal processes. | 5+ years proposal, grant, or contract experience preferably in research or pharma/CRO, excellent writing, budgeting, leadership, organizational and communication skills. | POSITION TITLE: PROPOSAL MANAGER, COMMERCIAL LOCATION: REMOTE US This position reports to our global HQ in Cambridge, MA, and is fully remote within the US. Travel is expected when needed and local candidates are preferred. TriNetX is a remote-friendly company but is currently only registered for employment in certain states. To be eligible for employment, you must reside in one of the following states: AZ, CA, CO, CT, DE, FL, GA, ID, IL, KY, MA, MD, ME, MI, MN, MO, MT, NC, NH, NV, NY, OH, OK, OR, PA, RI, SC, TX, UT, VA, VT, WA, WI Who we are: TriNetX was founded on the idea that incorporating real-world data results in better clinical trial design, improves the site selection and patient recruitment process and generates real-world evidence (RWE) to advance the collective understanding of human health. TriNetX collaborates with the majority of industry leaders, including 13 of the top 15 pharmaceutical companies, and is powered by an impressive network of 170 healthcare organizations across 30 countries. As a result of its reach and rapidly expanding network, TriNetX has become the market leader in protocol design, feasibility, and site selection. Researchers have leveraged the TriNetX network to analyze over 39,000 protocols, presented over 10,000 clinical trial opportunities to its healthcare members, and reduced site identification time in clinical trials by 50%. Currently, TriNetX healthcare organization members contribute access to a patient population of 400 million, representing over 40 billion clinical observations. With headquarters in Cambridge, Massachusetts, TriNetX is one of the fastest-growing, privately held companies in the area's life sciences corridor. What challenges we work on: TriNetX is the global health research network that optimizes clinical research and enables discoveries through the creation of real-world evidence. TriNetX combines real-time access to longitudinal clinical data with state-of-the-art analytics to answer complex research questions at the speed of thought. Each member of our community shares in the consolidated value of our global, federated health research network that connects clinical researchers to the patient populations which they are attempting to study. Who we are looking for: Our customer base, networks, and product offerings are growing rapidly, and we are expanding with the hiring of a Proposal Manager, Commercial, to manage and develop proposals in Real-World Evidence (RWE) Consulting and other areas. Successful candidates will have a previous experience in proposal, grant, or contract development with a collaborative, can-do attitude and experience building relationships with both internal and external stakeholders. What you will be doing: • Supports our rapidly growing business with proposal development expertise • Ensures completion of on-time, high-quality proposal submissions to clients • Works directly with the commercial team and clients to understand service needs, which will inform customized, impactful proposals • Leads and contributes to the writing of proposals such as the project summary, background, deliverables, timeline, risks, cost and pricing and other sections as deemed necessary • Leads and contributes to the development of budgets and invoice schedules • Prepares regular reports on the progress and forecast of proposals to internal and external stakeholders using key metrics • Creates, evolves, and supports internal processes for pre-award activities including proposal scoping, budgeting, standard operating procedures, best practices, and other resources and templates as needed • Acquires a thorough understanding of our services to successfully position solutions and help ensure appropriate scope and budget • Makes effective decisions when presented with multiple options, and/or conflicting priorities • Uses influencing skills to accomplish successful proposal submissions - moving key proposal contributors (including senior executives) to meet agreed upon submission dates • Communicates with the senior leadership team to keep the proposals aligned with enterprise strategic goals What you bring to TriNetX: • A Bachelor`s or Masters degree and at least 5+ years of proposal, grant, or contract experience, preferably in research and/or pharmaceutical/CRO space, including budget development • Excellent writing and editing • Strong attention to detail • Inquisitive and willing to ask questions • Excellent organization skills • Proven leadership skills in a matrixed organization • Excellent communication, interpersonal and negotiation skills • Ability to prioritize and make important decisions under pressure • Self-motivated, team-oriented, and deadline-driven • Problem-solving skills • Time management skills Bonus points: • Understand how data (electronic health records, claims, real-world data) is used by the pharma/CRO industry • Knowledge of health outcomes research As a condition of employment, the individual must provide proof of Covid 19 vaccination unless a medical or religious exemption is granted by TriNetX. Learn more about TriNetX: Please feel free to check out our website www.trinetx.com and our careers page www.trinetx.com/careers/ to learn more. We are social and you can follow us on Twitter @TriNetX, LinkedIn https://www.linkedin.com/company/trinetx, The Muse https://www.themuse.com/profiles/trinetx and be sure to read our blog https://trinetx.com/blog/ Interested in joining our community? TriNetX is an Equal Opportunity Employer. All persons are considered for employment without regard to their race, color, creed, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex or gender, marital status, sexual orientation, genetic information, gender identity, veteran status, or any other characteristic or status protected by applicable federal, state or local laws. This Organization Participates in E-Verify This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9. E-Verify Works for Everyone For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS. 888-897-7781 https://www.e-verify.gov/