<p>Why Sarepta? Why Now?</p> <p>The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.</p> <p>We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.</p> <p>What Sarepta Offers</p> <p>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:</p> <ul> <li> <p>Physical and Emotional Wellness</p> </li><li> <p>Financial Wellness</p> </li><li> <p>Support for Caregivers</p> </li></ul> <p>For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us</p> <p>The Importance of the Role</p> <p>We are seeking a Senior Manager who will be responsible for the project management of advisory board meetings to support the execution of Sarepta's Advisory Board Plan, as well as other opinion leader engagements. This individual will be key in collaborating with cross functional partners (Medical Affairs, Clinical Development, etc.) to determine and develop the scientific content that will be shared at advisory boards to ensure robust feedback on Sarepta's objectives. This individual should have a strong understanding of the biotech environment for rare diseases and deep therapeutic knowledge of the mechanism of action of the different precision genetic medicines offered by Sarepta commercially and in clinical development.</p> <p>The Opportunity to Make a Difference</p> <ul> <li> <p>Project management of advisory board meetings to support execution of strategic plan</p> </li><li> <p>Development of project timelines and management of workstreams to support timely execution</p> </li><li> <p>Liaising with cross-functional stakeholders to support content development and related workstreams according to timelines</p> </li><li> <p>Oversight of vendors to support advisory board activities</p> </li><li> <p>Management of documentation related to HCP engagements and advisory board meetings</p> </li><li> <p>Ensuring adherence to Compliance requirements for HCP engagements</p> </li><li> <p>Have an in-depth understanding of RNA therapeutics, gene therapy, and siRNA-based treatments</p> </li><li> <p>Serve as a product expert and share KOL insights as a member of GBTs & GPTs</p> </li><li> <p>Lead the creation and review of high-quality scientific content for advisory board materials</p> </li><li> <p>Identify opportunities for program enhancement and provide strategic input to cross-functional teams.</p> </li></ul> <p>More about You</p> <ul> <li>PharmD, PhD, or advanced science degree REQUIRED </li><li>5+ years of experience in rare disease biotech </li><li>Proven track-record of project management skills </li><li>Excellent written and verbal communication skills, with a sharp eye for scientific detail and narrative flow </li><li>Ability to manage multiple projects and priorities in a fast-paced environment </li><li>Highly proficient in Microsoft Office suite (Outlook, Excel, Word, PowerPoint, Visio) </li></ul> <p>What Now?</p> <p>We're always looking for solution-oriented, critical thinkers.</p> <p>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.</p> <p>#LI-Hybrid</p> <p>#LI-TD1</p> <p>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.</p> <p>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.</p> <p>Candidates must be authorized to work in the U.S.</p> <p>Sarepta Therapeutics offers a competitive compensation and benefit package.</p> <p>Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.</p>