Medical Science Liaison - New England Territory

Sarepta Therapeutics; Maryland; Remote; USD 100,000 - 160,000; Full time

Job summary

An established industry player is seeking a dedicated Medical Science Liaison to enhance education on Duchenne Muscular Dystrophy and Limb Girdle Muscular Dystrophy. This role emphasizes building relationships with healthcare professionals while providing scientific insights into investigational therapies. Candidates should possess a strong scientific background, excellent communication skills, and a passion for improving patient outcomes. This position offers the opportunity to work remotely while also engaging with the community through in-person events. Join a mission-driven team committed to transforming lives through innovative genetic medicine.

Benefits

Physical and Emotional Wellness Support

Financial Wellness Resources

Support for Caregivers

Qualifications

• 5+ years of MSL experience preferred, with familiarity in Neurology/Pediatrics.
• Strong communication and presentation skills essential for the role.

Responsibilities

• Educate healthcare professionals about Duchenne and Limb Girdle Muscular Dystrophy.
• Develop relationships with key opinion leaders and support clinical trials.

Skills

Scientific Knowledge

Customer Service

Communication Skills

Presentation Skills

Negotiation Skills

Team Collaboration

Education

MD, PhD, PharmD, or NP/PA

Tools

Clinical Trial Design

Competitive Intelligence Tools

Drug Information Systems

Job description

Medical Science Liaison - New England Territory

Medical Science Liaison - New England Territory

Apply remote type Remote locations New England (Field) time type Full time posted on Posted 2 Days Ago job requisition id R-02892

Why Sarepta? Why Now?
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.

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

The Importance of the Role

The MSL will play a pivotal role in the education of healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Limb Girdle Muscular Dystrophy as well as Sarepta’s investigational therapeutics and product pipeline. Reporting to the East Region Team Leader, the MSL position will play a pivotal role in the education of healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Limb Girdle Muscular Dystrophy as well as Sarepta’s investigational therapeutics and product pipeline. The incumbent is expected to have expertise in the field of Neurology / Pediatrics and to be a scientific expert regarding Sarepta’s portfolio of products. 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 a highly driven individual who combines scientific knowledge with a focus on customer service and compassion for the patients we serve. The person in this position will also need to be willing to actively contribute to the establishment of MSL process and policy, KOL strategy development, and tactical planning.

This position requires the incumbent to be located in New England and covering territory of the following states: MA, CT, RI, NH, ME, VT and upstate NY.

The Opportunity to Make a Difference

• 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.
• Leadership role in medical education for healthcare professionals through proactive communication of scientific data as well as scientific exchange of information during routine interactions.
• High quality presentations of scientific data to health care professionals in various settings, including advisory boards, investigator meetings, and other appropriate venues to enhance product / disease state knowledge.
• Provide on-site support to clinical operations for investigators in ongoing clinical trials, investigator-initiated studies, and registries consistent with company objectives and regulations.
• Visit potential sites to assess their capabilities with regard to conduct these various forms of clinical research.
• 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 with medical information 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.
• Demonstrate an understanding of key medical and commercial strategies and provide medical support for commercial activities.

More about You

• MD, PhD, PharmD, or NP/PA preferred.
• 5+ years of MSL experience a plus.
• Familiarity with and track record of complying with industry and regulatory compliance guidelines.
• Demonstrated ability to work independently and in a collaborative team environment.
• Existing Neurology / Pediatric experience and relationships is a plus, experience in immunology and/or gene therapy a plus.
• Willingness to travel >50% of time.
• Experience and expertise in clinical trial design, interpretation of scientific data, competitive intelligence tools, drug information systems, and medical marketing strategies.
• 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.

This position is remote. However, 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 $0 - $0 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.

About Us

Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. 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. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing.