Senior Medical Science Liaison - Southeast

Role Summary

Senior Medical Science Liaison - Southeast. Role focuses on education of healthcare professionals about Duchenne Muscular Dystrophy and Sarepta’s investigational therapeutics and product pipeline. Requires expertise in Neurology / Pediatrics and acts as a scientific resource for key customers, contributing to MSL processes, KOL strategy, and tactical planning. Candidates must reside in the Southeast region (preferably Alabama, Georgia, or Florida).

Responsibilities

• Identify, establish, and maintain collaborative relationships with key opinion leaders, investigators, and institutions within academic, clinical, and health care organizations in a defined territory
• Implement KOL field strategy, KOL identification, speaker development, and support
• Lead medical education for healthcare professionals through proactive communication of scientific data and exchange of information during routine interactions
• Deliver high quality presentations of scientific data to healthcare professionals in various settings to enhance product/disease state knowledge
• Provide on-site support to clinical operations for investigators in ongoing clinical trials, investigator-initiated studies, and registries complying with company objectives and regulations
• Visit potential sites to assess capabilities for conducting these forms of clinical research
• Represent and support medical affairs at global, national, and regional scientific meetings, including staffing booths, gathering competitive intelligence, and developing post-conference scientific materials with medical information
• Develop and maintain clinical expertise in Duchenne muscular dystrophy through review of scientific journals, data disclosures, and participation in congresses
• Demonstrate understanding of medical and commercial strategies and provide medical support for commercial activities

Qualifications

• MD, PhD, PharmD, or NP/PA preferred
• 5+ years of MSL experience is a plus
• Familiarity with and track record of complying with industry and regulatory guidelines
• Ability to work independently and in a collaborative team environment
• Neurology/Pediatric experience and relationships is a plus; experience in immunology and/or gene therapy is a plus
• Willingness to travel >50% of the time
• Experience in clinical trial design, interpretation of scientific data, competitive intelligence tools, drug information systems, and medical marketing strategies
• High integrity, sense of urgency, and ability to recognize time sensitivity
• Excellent written and verbal communication, listening, presentation, and negotiating/influencing skills

Skills

• Scientific prowess in neurology/pediatrics
• Medical affairs and KOL engagement
• Clinical trial operations support
• Scientific communication and presentation
• Strategic planning and policy development within MSL scope

Education

• MD, PhD, PharmD, or NP/PA preferred

Additional Requirements

• Hybrid work arrangement with on-site presence at Sarepta facilities and occasional in-person events
• Authorized to work in the U.S.