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Midwest, Wyoming, United States
Hybrid
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 Medical Science Liaison (MSL) plays a pivotal role in establishing and fostering peer-to peer relationships with healthcare professionals (HCPs) involved in the management of neuromuscular diseases in line with Sarepta’s marketed and investigational product pipeline.The Opportunity to Make a Difference
Identifies, establishes, and fosters peer-to-peer relationships with Key Opinion Leaders (KOLs), clinicians and researchers within disease state areas aligned to Sarepta's marketed and investigational products, e.g. neuromuscular experts
Develops and implements rolling and goal-oriented KOL field engagement strategy that demonstrates ownership of the execution of the medical strategy, projects and initiatives with their region.
Demonstrates strong knowledge of disease-state and product/platform data through communication of complex clinical data and product information in a clear, compliant, and non-promotional manner
Collects high quality, actionable feedback and reports trends and unmet medical needs, leading to strategic impact
Deliver high-quality presentations of scientific data to health care professionals in various settings, including peer-to-peer meetings, advisory boards, investigator meetings, and other appropriate venues to enhance product / disease state knowledge
Supports investigator-initiated studies (IIS/SRA), regional research collaborations, registries, and other evidence generation activities. Assesses site capabilities with regard to the effective conduct of these various forms of clinical research, providing feedback to internal teams.
Provide professional medical affairs representation and support at global, national and regional scientific meetings, including but not limited to staffing medical affairs booths, gathering competitive intelligence, and partnering to develop post-conference scientific materials
Develop and maintain clinical expertise in Duchenne muscular dystrophy through review of scientific journals, recent data disclosures and participation in scientific congresses
Maintain strong working relationships with cross-functional field, GMA peers, and other internal teams to provide a compliant, coordinated approach to engagement and effective project management and execution
Completes all MSL administrative tasks (Veeva, Concur, compliance wire etc.), initiatives, and projects on time
More about You
Graduate level degree (MD, PhD, PharmD) or equivalent required
Minimum of 3 years of work experience in research and development, clinical trials, medical information, clinical practice, or other related position(s) pertinent to our therapeutic areas; Medical Affairs / MSL experience preferred.
Demonstrates strong emotional intelligence, optimism, and a solutions-oriented mindset
Proven ability to effectively communicate advanced concepts to stakeholders
Familiarity with and track record of complying with industry and regulatory compliance guidelines
Demonstrated ability to work independently and in collaborative team environment
Willingness to travel >50% of time
Experience and expertise in clinical trial design / execution and interpretation of scientific data
High integrity, sense of urgency, ability to recognize time sensitivity
Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills
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.
