Sarepta Therapeutics, Inc.

Manage and execute components of the global compliance program, including training, monitoring, risk assessment, and standards management. | Minimum 7 years in the pharmaceutical, biotech, or medical device industry with at least 4 years in compliance responsibilities, strong project management and communication skills. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role Senior Manager, Global Compliance Operations will report to the Senior Director, Head of Global Compliance Operations and is a great opportunity for a highly motivated individual who is interested in independently managing critical components of the Compliance program in a dynamic and fast paced environment. This role requires strong attention to detail, professionalism, sound judgement, and the ability to work cross functionally with multiple stakeholders. The Opportunity to Make a Difference This role is responsible for executing tasks and initiatives that span all three pillars of Sarepta’s Global Compliance Program. The successful candidate will contribute to activities supporting Global Healthcare Compliance, Global Data Privacy and Data Management, and Global Sanctions and Trade Controls, as described below. Training: Work with manager to develop the annual training plan based on risk assessment Support, prepare, and conduct Compliance trainings as needed based on business activity or part of monitoring remediation Works with HR to distribute annual eLearning modules and track to completion Works with HR to distribute annual policies and track to completion Works with Corporate Communications to distribute annual Compliance Minutes Video series Responds to internal audit request for training statistics Monitoring and Auditing plan: Work with manager on the development of the annual monitoring plan based on the risk assessment Live and desktop monitoring Live co-travels with field team Reviews and analyzes monitoring and auditing results twice a year to test the effectiveness of the Compliance program Leverages transparency data to test key internal controls and inform the risk-based monitoring plan Risk Assessment: Supports manager in the annual review of company risks based on activities Written Standards: Assists in the annual review of all written standards as needed Management of Compliance Tools: Tiering & FMV tool including adding more countries and specialties as requested by the business Needs Assessment Forms Maintenance of Workday Learning resources lifecycle Nucleus page Maintains all user guides associated with tools Other Leads or participates in other key initiatives as requested. More about You Bachelor’s degree required. Minimum of 7 plus years of relevant experience in the pharmaceutical, biotech, or medical devices industry with four years of direct compliance responsibilities. Strong planning and project management skills. Strong computer software skills (Microsoft Office Suite – Word, Excel, PowerPoint, and Visio); ability to manage databases and generate meaningful tables and charts for executive presentations. Team player with a high level of interpersonal skills and collaborative working style to effectively work cross-functionally within the company. Strong verbal and written communication skills, including ability to communicate with a wide range of individuals and constituencies in a diverse community. Ability to prioritize multiple tasks and meet deadlines. What Now? We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Hybrid #LI-ES1 This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time. The targeted salary range for this position is $136,000 - $170,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify. Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. Our deep pipeline is driven by our multi-platform technologies in siRNA, RNA and gene therapy. For more information, please visit www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook.

Leading design and system development for rockets, collaborating on electronic and propulsion systems, and building prototypes. | Currently pursuing a Bachelor's in Mechanical Engineering with skills in CAD, circuit design, and programming; no direct experience in biotech or automation systems. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. The Importance of the Role The Intern, High Throughput Process Automation, will play a key role in advancing Sarepta's high throughput workflows that support upstream, downstream, and analytical development within the Early Research & Process Development (ERPD) organization. This internship represents an exceptional opportunity for a student interested in biotech R&D to gain hands on experience with advanced automation technologies, including Tecan Fluent liquid handling systems, automated tangential flow filtration platforms, and high throughput purification modalities. The intern will work in a highly collaborative, cross functional environment, and will contribute to activities that directly impact Sarepta's ability to generate critical research materials (Fabs, mAbs, proteins, and other biologics) for internal chemistry and biology partners. They will also play a key role in process development efforts for early-stage research programs. This role offers scientific mentorship, including support from team members experienced in academic and industry training. The Opportunity to Make a Difference In this role, the intern will have the opportunity to: • Develop, test, and optimize workflows for the Autopulse automated tangential flow filtration instrument, enabling efficient buffer exchange and concentration of multiple therapeutic modalities (Fab, Mab, proteins, and oligo conjugates). • Perform experimental design, execution, and data analysis to establish high-quality TFF workflows following ERPD pipeline updates. • Support downstream process development efforts using Tecan Fluent systems in both RoboColumn and batch filter plate formats to generate critical purification data for upstream and downstream development teams. • Set up, execute, and troubleshoot high throughput purification experiments to accelerate development timelines across ERPD. • Collaborate closely with upstream, downstream, and analytical development groups, gaining exposure to multiple scientific disciplines and technologies. • Document experimental execution and results to enhance team knowledge sharing and process reliability. • Contribute to continuous improvement initiatives by identifying opportunities to improve workflow efficiency, automation robustness, and interteam collaboration. More about You • Current undergraduate or graduate student in Chemical Engineering, Bioengineering, Biochemistry, Biotechnology, Biology, or related scientific discipline. • Strong interest in laboratory research, bioprocess development, or automation enabled experimentation. • Comfort working with complex instrumentation and a willingness to learn new automated systems and workflows. • Strong analytical, problem-solving, and documentation skills. • Ability to thrive in a collaborative team environment and communicate effectively with peers and mentors. • Demonstrated curiosity, attention to detail, and motivation to improve laboratory processes. Preferred Qualifications • Prior hands on experience with laboratory automation, liquid handlers (e.g., Tecan), or filtration systems is a plus. • Experience working with proteins, antibodies, or viral vectors in an academic or industry setting. • Familiarity with chromatography, filtration, or other downstream purification techniques. Program Timeline This application is for a 12-week summer internship program that will start on May 18th and conclude on August 7th, 2026. What Now? We're always looking for solution-oriented, critical thinkers. So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-OnsiteBlank This position requires work on site at one of Sarepta's facilities in the United States. The targeted salary range for this position is $21 - $26 per hour depending upon years of education completed and nature of role. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

Support laboratory operations, manage reagents and inventory, ensure compliance, and collaborate with cross-functional teams. | Extensive experience in molecular biology, biochemistry, or chemistry, with specific expertise in gene expression analysis and laboratory operations, preferably in a regulated industry. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role Reporting to the Sr. Director of QC Operations, the Associate Director of QC operations is responsible for supporting the operations of the internal ddPCR, qPCR and Cell-based assays. The individual will be responsible for supporting all aspects of the laboratory and facility footprint including safety, compliance, instrumentation and equipment qualification and maintenance. Prior experience with laboratory expansion projects is beneficial. This role is responsible for inventory management, raw material procurement as well as the qualification and bridging of critical reagents needed to support internal and external testing at our CMO/CTL partners. The Associate Director of QC Ops is responsible for the supervision of laboratory ops personnel and the optimization of department resource allocation according to project/program needs to assure activities occur in an efficient, safe, timely and cGMP compliant manner. The Opportunity to Make a Difference Manage the inventory for all reference standards, assay controls and critical reagents qualification, bridging, and expiration extension Generate Certificate of Analysis for critical reagents in compliance with cGMP Monitoring KPIs associated with laboratory performance, productivity, run time and efficiency Establish cross-functional relationships with Sarepta CMC stakeholders to aligned goals, timelines, and resource requirements Establish and manage external collaborations to accomplish key Sarepta objectives Proactively identify opportunities to improve operational efficiency, communication, and program outcomes Ensures compliance with GCP, GLP and cGMP guidelines both internally at Sarepta and at contract testing laboratories Procure new equipment and support timelines for qualification Support quality events associated with Laboratory investigations, deviations, change controls, etc. Author regulatory submission sections and address questions from health authorities regarding critical reagents Manage spend through budget planning, Scope of Work requests, invoice reconciliation, and change orders More about You MS/BS in Molecular Biology, Biochemistry, Chemistry with 8+ years relevant industry experience required Direct working experience in AAV products is highly desired. Extensive technical expertise with gene expression analysis including qRT-PCR, ddPCR, and immunoassays such as Jess capillary electrophoresis, ELISA, immunoblotting. Experience operating liquid handlers is beneficial. Proven ability to balance conflicting priorities across multiple programs, and to make sound recommendations for trade-offs to achieve aligned objectives. Strong interpersonal skills and a proven ability to communicate effectively through verbal and written formats. Laboratory expansion experience is beneficial Self-starter with the ability to work in a fast-paced, cross-functional, highly collaborative environment. What Now? We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Onsite #LI-ES1 This position requires work on site at one of Sarepta’s facilities in the United States. The targeted salary range for this position is $160,800 - $201,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify. Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. Our deep pipeline is driven by our multi-platform technologies in siRNA, RNA and gene therapy. For more information, please visit www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook.

Lead market research, competitive intelligence, and insights to support commercial brand planning and new product launches in a cross-functional biopharma environment. | 15+ years in brand marketing/strategy, market research, analytics, or competitive intelligence with 5+ years in biopharma, strong project management, and new product launch experience. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: • Physical and Emotional Wellness • Financial Wellness • Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role The Senior Director, Market Research, CI, Insights is responsible for ensuring actionable recommendations and solutions that support the launch and commercial success of Sarepta's current platform and other pipeline products. The role involves maintaining timelines, industry knowledge, market alerts, conference coverage, primary market research, and Leadership briefings on competitive events as they occur. This position partners with Brand teams to ensure effective and impactful leverage of market research, competitive intelligence, and analytics initiatives. This position also partners with several functions throughout the organization to ensure consistency and awareness, including Medical Affairs, Corporate Strategy, New Product Planning, and Marketing. As a member of the Commercial Operations department, the Senior Director also partners with Analytics, Forecasting and Commercial & Medical field teams to generate action-oriented business insights, communicate effectively and drive pull-through of the actions. The Opportunity to Make a Difference • Shape the strategy of the Gene Therapy and RNA business by developing a robust, cross-functional insights generation program, in collaboration with internal partners. • Develop, execute and disseminate primary and secondary market research supporting commercial brand planning, demand forecasting, and insights generation. • Utilize multiple and creative sources of market research to form the groundwork for strategy to better understand and anticipate customer needs. • Develop strong cross-functional relationships with other team members (marketing, sales, analytics, market access, medical affairs, patient services). • Lead the Competitive Intelligence function for the Customer organization - synthesizing sources, information, and points of view into an aligned, clear repository. • Manage external vendor resources to track market events and conduct primary market research. • Manage the collection and dissemination of competitive intelligence across multiple platforms partnering with external suppliers and internal stakeholders. • Manage external CI online portal - including design, content, and distribution. • Ensures Sarepta's adherence and compliance with all appropriate industry and company standards as it relates to Competitive Intelligence. • Leads ongoing forum for competitive intelligence sharing across the organization. • Maintains process of alerting key stakeholders to market events and developments. • Manage relationships with external market research, competitive intelligence, and analytics suppliers. • Manage brand-level Insights budget and project plan. • Other related duties as required. More about You • Bachelor's Degree required, Master's Degree strongly preferred. • 15+ years' experience in some combination of the following; Brand marketing/strategy, Market research, Business analytics, Competitive intelligence with at least 5+ years of experience in the biopharmaceuticals industry. Rare Disease market experience is a plus. • Strong project management experience with the ability to work on multiple projects simultaneously. • Excellent communication and analytical skills. • New product launch experience. What Now? We're always looking for solution-oriented, critical thinkers. So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Hybrid #LI-ES1 This position is hybrid, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time. The targeted salary range for this position is $216,000 - $270,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

Lead and manage market research, competitive intelligence, and insights programs to support product launches and commercial success, collaborating cross-functionally and managing external vendors and budgets. | 15+ years in market research, brand marketing, business analytics or competitive intelligence with 5+ years in biopharmaceuticals, strong project management, new product launch experience, and advanced degree preferred. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role The Senior Director, Market Research, CI, Insights is responsible for ensuring actionable recommendations and solutions that support the launch and commercial success of Sarepta’s current platform and other pipeline products. The role involves maintaining timelines, industry knowledge, market alerts, conference coverage, primary market research, and Leadership briefings on competitive events as they occur. This position partners with Brand teams to ensure effective and impactful leverage of market research, competitive intelligence, and analytics initiatives. This position also partners with several functions throughout the organization to ensure consistency and awareness, including Medical Affairs, Corporate Strategy, New Product Planning, and Marketing. As a member of the Commercial Operations department, the Senior Director also partners with Analytics, Forecasting and Commercial & Medical field teams to generate action-oriented business insights, communicate effectively and drive pull-through of the actions. The Opportunity to Make a Difference Shape the strategy of the Gene Therapy and RNA business by developing a robust, cross-functional insights generation program, in collaboration with internal partners. Develop, execute and disseminate primary and secondary market research supporting commercial brand planning, demand forecasting, and insights generation. Utilize multiple and creative sources of market research to form the groundwork for strategy to better understand and anticipate customer needs. Develop strong cross-functional relationships with other team members (marketing, sales, analytics, market access, medical affairs, patient services). Lead the Competitive Intelligence function for the Customer organization – synthesizing sources, information, and points of view into an aligned, clear repository. Manage external vendor resources to track market events and conduct primary market research. Manage the collection and dissemination of competitive intelligence across multiple platforms partnering with external suppliers and internal stakeholders. Manage external CI online portal – including design, content, and distribution. Ensures Sarepta’s adherence and compliance with all appropriate industry and company standards as it relates to Competitive Intelligence. Leads ongoing forum for competitive intelligence sharing across the organization. Maintains process of alerting key stakeholders to market events and developments. Manage relationships with external market research, competitive intelligence, and analytics suppliers. Manage brand-level Insights budget and project plan. Other related duties as required. More about You Bachelor’s Degree required, Master’s Degree strongly preferred. 15+ years’ experience in some combination of the following; Brand marketing/strategy, Market research, Business analytics, Competitive intelligence with at least 5+ years of experience in the biopharmaceuticals industry. Rare Disease market experience is a plus. Strong project management experience with the ability to work on multiple projects simultaneously. Excellent communication and analytical skills. New product launch experience. What Now? We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Hybrid #LI-ES1 This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time. The targeted salary range for this position is $216,000 - $270,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify. Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. Our deep pipeline is driven by our multi-platform technologies in siRNA, RNA and gene therapy. For more information, please visit www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook.

Educate healthcare providers, patients, and caregivers on Duchenne therapies, provide infusion support, conduct disease awareness programs, and perform on-call triage nursing support. | Bachelor’s degree in nursing, 5+ years relevant clinical experience, bilingual English/Spanish, pharmaceutical industry experience preferred, ability to travel extensively, and on-call availability. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role The Duchenne Nurse Educator (DNE) works in a highly visible, dedicated team environment. The bilingual (English/Spanish) speaking DNE will support health care providers (HCPs), patients, and caregivers through education on Duchenne Muscular Dystrophy (DMD), the infusion process of our approved therapies, and Sarepta patient support programs. This role develops relationships with HCP’s, patients, and caregivers to support both the HCP’s and the families through their journey on therapy. The DNE also collaborates closely with their cross functional partners to ensure ongoing compliance with therapy. This position will cover Washington, Oregon, Northern California, Montana, Idaho, Wyoming, Alaska. The DNE is assigned to special projects as required, such as providing nurse triage support during 24-hour on-call shift coverage. Triage support utilizes the nursing process to liaise with patient care teams to evaluate patient safety needs over the telephone. On this special project, the DNE serves as a connection between patient care teams and an experienced physician with deep Duchenne and precision medicine expertise and provides in the moment guidance to patient care teams, if needed, while adhering to organizational policies, procedures, and guidelines. The Opportunity to Make a Difference The bilingual (English/Spanish) speaking DNE will educate providers, infusion nurses, patients, and caregivers on Sarepta’s approved therapies for DMD and the infusion process. Serve as recognized expert on DMD education (Genotype, deletions, disease process, etc.) Stay current on the DMD environment. Collaborate with internal cross functional partners and external partners to ensure ongoing support to HCP’s patients, and families. Present to audiences compliantly. Conduct Programs for disease state awareness. Assist to improve infusion experience for DMD patients by providing ongoing support to the infusion nurses and sharing best practices. Work with SareptAssist team and specialty pharmacy to ensure smooth transition from infusion center to home infusion for PMO therapies. Support to patients and families as requested by case manager or health care provider. Attend advocacy meetings and represent Sarepta at industry conferences. Travel to training meetings, medical offices, and home health agencies, as necessary. Other related duties as required. Special projects including triage nursing support: Triage telephone calls from patient care teams requiring medical guidance post gene therapy treatment during rotating 24-hour on-call shifts. Intake and interpret different nuances of medical information to triage calls appropriately. Communicates and acts as a liaison between patient’s care teams and an experienced physician in a confidential manner. Documents calls according to established guidelines (PV reporting). Directs the patient care team to the proper Customer Service Center (e.g., Medical information, SareptAssist) based on the topic of the call. Requires on call coverage to provide day, night, and weekend coverage. More about You Registered Nurse with a bachelor’s degree (BSN/BS/BA) from an accredited school. At least 5 years of relevant experience; Infusion, Neuromuscular, Pediatric Neurology, or other specialty experience preferred. Bilingual (English/Spanish) required. Ability to communicate effectively in both English and Spanish supports our efforts to better serve a diverse customer/client/community base. Prefer 2 or more years’ experience in the pharmaceutical/biotech industry. Highly interested in educating people on the disease state of Duchenne and working with health care professionals to support patients and families. Exceptional presentation, verbal, and written communication skills Demonstrates team-based skills collaborating with cross functional partners, both internally and externally. Competent and comfortable presenting in group and individual settings, live and virtually, with and without technology. Empathetic, friendly, and relatable, with effective communication skills. Comfortable speaking with patients/families. Willingness to work as part of a team in a demanding environment. Embraces continuous learning/seeks knowledge. Valid driver’s license and in good standing. Requires rotating on call coverage 24 hours/7 days per week. Ability to travel, including ground and air transportation, up to 60% within assigned territory is required. Must be able to travel to meetings, training, and other programs, as necessary. What Now? We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Hybrid #LI-ES1 This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time. The targeted salary range for this position is $132,000 - $165,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify. Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. Our deep pipeline is driven by our multi-platform technologies in siRNA, RNA and gene therapy. For more information, please visit www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook.

Lead cross-portfolio medical communication strategy and deliverables including symposia, publications, digital assets, and stakeholder collaboration. | Advanced scientific degree (PhD or PharmD preferred) with 5+ years scientific communications experience, knowledge of industry guidelines and regulations, and strong organizational and communication skills. | Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role The Senior Manager, Global Scientific Communications – Cross-portfolio is responsible for the development of high-quality, fair-balanced, scientifically accurate medical communication deliverables and pipeline publications in accordance with established timelines, compliance guidelines, and budgets. The Senior Manager is actively involved in the creation of cross-portfolio medical communication strategy and activities including but not limited to company sponsored symposia, digital assets, and slide decks. This role manages the development and review/approval of assigned projects, according to timelines and communicates effectively with internal and external stakeholders. The Opportunity to Make a Difference Assist in the implementation of a strategic cross-portfolio medical communication plan. Lead strategy, planning, content development and related activities for Sarepta-sponsored symposia at scientific congresses. Support pre- and post-launch medical communication deliverables. Lead the development and maintenance of slide-decks, medical-booth materials, and other digital assets for use at scientific congresses. Support content development and approval process for Invited Presentations/Talks by internal Sarepta employees. Serve as lead on assigned pipeline scientific publications (abstracts, posters, presentations, and manuscripts) and work with authors, evidence generation teams, and medical communication agencies on the timely execution of publication plans, ensuring a high quality and timely product, as well as adherence to publication SOP and associated procedures. Support development and revision of publication plans and cross-functional alignment across relevant internal stakeholders for assigned pipeline products in line with program strategies and priorities. Review draft pipeline publications for scientific quality, data accuracy, and ensure alignment with author direction. Assist with digital initiatives (example: GMA medical website) ensuring successful evaluation, execution and utilization of these initiatives. Serve as Medical Communication lead on cross-functional team meetings and provide guidance on processes and practices as needed. Manage partner agencies on the timely execution of all medical communications related deliverables Support budget management. Perform other related duties as needed. More about You Advanced Scientific Degree (Ph.D., Pharm. D) with at least 5 years of relevant experience including postdoctoral training or fellowship experience. Master’s Degree will be considered with at least 7 years of significant scientific communications experience. Excellent organizational and communication (verbal and written) skills are essential; other required skills include attention to detail, strategic planning, multi-tasking and prioritizing. Ability to understand and interpret scientific data. Good understanding of industry guidelines associated with scientific publications. Knowledge of US and international regulations, requirements, and guidance’s associated with scientific data disclosures is required. Experience in rare disease/neurology preferred. Experience of working with fast-paced, collaborative, cross-functional teams. Ability to travel up to 20%. Must be proficient with Microsoft Windows, Word, Excel, and PowerPoint. Recognized by former peers/colleagues/managers for attributes congruent with Sarepta Cultural Values: Patients First, Action, Unconventional Thinking, Talent, and Integrity. Excellent organizational, interpersonal, and communications (verbal, written, presentation) skills with attention to detail. What Now? We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. #LI-Hybrid #LI-ES1 This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time. The targeted salary range for this position is $132,000 - $165,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S. Sarepta Therapeutics offers a competitive compensation and benefit package. Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify. Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. Our deep pipeline is driven by our multi-platform technologies in siRNA, RNA and gene therapy. For more information, please visit www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook.