Senior Manager, Scientific Communications at Sarepta Therapeutics

Cambridge, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

10 Apr, 26

Salary

165000.0

Posted On

10 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Scientific Communication, Publication Planning, Data Interpretation, Organizational Skills, Interpersonal Skills, Communication Skills, Attention to Detail, Medical Writing, Collaboration, Budget Management, Statistical Concepts, Microsoft Office, Cross-Functional Teamwork, Real-World Evidence, Healthcare Economics, Publication Management

Industry

Biotechnology Research

Description

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, Scientific Communications, will serve as the primary liaison for internal teams, internal/external authors, and publication agencies regarding all publication activities related to the assigned product. The individual in this role will possess strong knowledge of good publication practices, authorship guidelines (ICMJE), and other relevant industry standards to ensure the delivery of high-quality scientific publications (scientific abstracts, presentations, and manuscripts) in a timely and compliant manner. This role will manage the development and review/approval of assigned projects in accordance with timelines in the Global Health Outcomes, Real-World Evidence, and Access (GHRA) Communications Plan, communicate effectively with external authors and internal stakeholders, and provide project updates to the Director, Scientific Communications. The Opportunity to Make a Difference Support the development and revision of a strategic Sci Comms plan for the assigned therapeutic platform(s) as they relate to GHRA tactics including publication and congress plans Serve as the lead on publications (abstracts, posters, presentations, and manuscripts) and work with authors, evidence generation teams, and medical communication agencies to ensure the timely execution of publication plans, ensuring a high quality and timely product, as well as adherence to publication SOPs and associated procedures Review draft publications for scientific quality and data accuracy, and ensure alignment with author direction Present and review the assigned publication plan and conference data disclosures at internal cross-functional team meetings, as needed Interface with external experts (e.g., physicians, other health care professionals, health economists) and effectively collaborate with cross-functional teams Explore opportunities for publication enhancements (plain language summaries/plain language summary publications/infographics) for the assigned product to increase the value of publications in scientific exchange Communicate the publication development process and industry guidance on good publication practices and authorship criteria to team members as needed Manage publication agency partners and contractors in the execution of publication and scientific communications tactics Contribute to budget management, forecasting, and resource allocation for the assigned therapeutic platform(s); actively track publication expenditures and ensure that they are within the approved budget Contribute to relevant medical communication activities, which may include but are not limited to slide decks, internal medical training, and company-sponsored symposia content development Serve as the Sci Comms representative at relevant internal team meetings Attend scientific conferences and provide coverage support as assigned More about You An advanced Scientific Degree (Ph.D., PharmD) required. A Master’s Degree will be considered with significant publication planning and writing experience. Relevant professional certification/credential (e.g., CMPP, AMWA) is preferred At least 5 years of medical/scientific publication planning and development experience in the pharmaceutical/biotech industry or at medical communication agencies Ability to understand and interpret scientific data Excellent organizational, interpersonal, and communication (verbal, written, presentation) skills with flawless attention to detail Experience in the rare disease/neurology therapeutic area Familiarity with publications management databases such as iEnvision Experience developing HEOR, real-world evidence, or patient-reported outcomes publications Good understanding of industry guidelines related to scientific publications Working knowledge of statistical concepts Proficient in Microsoft Windows, Word, Excel, and PowerPoint Experience working with fast-paced, collaborative, cross-functional teams Ability to prioritize and support business-critical or emergent critical publications in response to evolving business needs 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.

Responsibilities

The Senior Manager, Scientific Communications will manage publication activities related to assigned products, ensuring high-quality scientific publications are delivered in a timely manner. This role involves collaboration with internal teams, external authors, and publication agencies to execute publication plans effectively.