Sarepta Therapeutics
Senior Medical Science Liaison - Texas
Sarepta Therapeutics, Houston, Texas, United States, 77246
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 supporting them in all aspects of their lives. We aim to maintain a culture that acknowledges people bring their whole selves to work, and we strive to help everyone integrate their work and personal lives while maintaining productivity. Our benefits and work-life resources support:
Physical and Emotional Wellness
Financial Wellness
Support for Caregivers
For a full list of our benefits, see:
https://www.sarepta.com/join-us The Importance of the Role The Senior MSL will play a pivotal role in educating healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Sarepta's therapeutics and pipeline. Reporting to the West Region Team Leader, the incumbent should have expertise in Neurology/Pediatrics and serve as a scientific resource for key customers, including opinion leaders, investigators, and physician networks. The candidate should be highly driven, combining scientific knowledge with customer service and compassion. They will also contribute to establishing MSL processes, policies, KOL strategy, and tactical planning. This position requires the candidate to be located in Texas or Oklahoma. The Opportunity to Make a Difference Establish and maintain relationships with key opinion leaders and institutions within the territory Implement KOL strategies, speaker development, and support Lead medical education efforts through proactive communication and scientific exchange Present scientific data effectively in various settings Support clinical operations for ongoing trials, investigator-initiated studies, and registries Assess site capabilities for clinical research Represent and support medical affairs at scientific meetings Develop clinical expertise in Duchenne muscular dystrophy Understand and support medical and commercial strategies More about You MD, PhD, PharmD, or NP/PA preferred 5+ years of MSL experience a plus Familiar with industry and regulatory compliance Ability to work independently and collaboratively Existing Neurology/Pediatrics relationships are a plus; experience in immunology or gene therapy is also beneficial Willing to travel >50% Experience in clinical trial design, data interpretation, and medical strategies High integrity, sense of urgency, and time management skills Excellent communication, listening, presentation, and influencing skills What Now? We seek solution-oriented, critical thinkers who are comfortable with ambiguity, challenge themselves, and prioritize kindness and integrity. If that describes you, we encourage you to apply. #LI-Hybrid #LI-CM1 This position is hybrid; you will work on-site at a Sarepta facility in the U.S. and attend company-sponsored events as needed. The salary range is $200,000 - $250,000 per year, commensurate with experience and other factors. Candidates must be authorized to work in the U.S. Sarepta offers a competitive benefits package. We are an Equal Opportunity/Affirmative Action employer and participate in e-Verify.
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https://www.sarepta.com/join-us The Importance of the Role The Senior MSL will play a pivotal role in educating healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Sarepta's therapeutics and pipeline. Reporting to the West Region Team Leader, the incumbent should have expertise in Neurology/Pediatrics and serve as a scientific resource for key customers, including opinion leaders, investigators, and physician networks. The candidate should be highly driven, combining scientific knowledge with customer service and compassion. They will also contribute to establishing MSL processes, policies, KOL strategy, and tactical planning. This position requires the candidate to be located in Texas or Oklahoma. The Opportunity to Make a Difference Establish and maintain relationships with key opinion leaders and institutions within the territory Implement KOL strategies, speaker development, and support Lead medical education efforts through proactive communication and scientific exchange Present scientific data effectively in various settings Support clinical operations for ongoing trials, investigator-initiated studies, and registries Assess site capabilities for clinical research Represent and support medical affairs at scientific meetings Develop clinical expertise in Duchenne muscular dystrophy Understand and support medical and commercial strategies More about You MD, PhD, PharmD, or NP/PA preferred 5+ years of MSL experience a plus Familiar with industry and regulatory compliance Ability to work independently and collaboratively Existing Neurology/Pediatrics relationships are a plus; experience in immunology or gene therapy is also beneficial Willing to travel >50% Experience in clinical trial design, data interpretation, and medical strategies High integrity, sense of urgency, and time management skills Excellent communication, listening, presentation, and influencing skills What Now? We seek solution-oriented, critical thinkers who are comfortable with ambiguity, challenge themselves, and prioritize kindness and integrity. If that describes you, we encourage you to apply. #LI-Hybrid #LI-CM1 This position is hybrid; you will work on-site at a Sarepta facility in the U.S. and attend company-sponsored events as needed. The salary range is $200,000 - $250,000 per year, commensurate with experience and other factors. Candidates must be authorized to work in the U.S. Sarepta offers a competitive benefits package. We are an Equal Opportunity/Affirmative Action employer and participate in e-Verify.
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