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Medical Science Liaison

About the position

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 candidate will have expertise in the field of Neurology / Pediatrics and be a scientific expert regarding Sarepta’s portfolio of products. The MSL will serve as a resource for scientific information for key customers, including but not limited to national and regional opinion leaders, investigators, advisors, and physician networks. The successful candidate will be highly driven individual who combines scientific knowledge with customer service, business acumen, and compassion for the patients we serve. This position requires extensive travel and requires the candidate to be located in IL/MI/IN/WI and covering a territory of the following states: IL/MI/IN/WI.

Responsibilities

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

Requirements

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
Candidates must be authorized to work in the U.S.

Benefits