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Zevra Therapeutics, Inc. is seeking a Senior/Principal Medical Science Liaison to join our U.S. Medical Affairs team in the Southeast/Southwest region. The role focuses on scientific exchange, KOL engagement, and evidence generation for rare diseases with our portfolio.
The successful candidate will translate complex clinical data into meaningful dialogue, build long-term collaborations, and travel regularly to meet with stakeholders while ensuring compliance and scientific integrity.
Zevra Therapeutics, Inc. Charlotte, North Carolina, United States
About Zevra Therapeutics, Inc.
We are a rare disease therapeutics company leading with science to make life-changing therapeutics available to patients with significant unmet needs. We involve key thought leaders, physicians, patients, care partners, and advocacy groups in all of our clinical and regulatory development strategies.
With a keen understanding that drug development often requires creative solutions, we have the insight and expertise to forge new pathways to success that others have missed. By following the data without bias, our transparent narratives and common-sense perspective have successfully overcome complex development challenges to make much-needed therapies available to patients.
Nimble and dauntless, we push boundaries beyond what is thought to be possible and advance new therapies that have the potential to bring meaningful improvement to patients’ lives.
Zevra Therapeutics is seeking a Senior Medical Science Liaison (Senior MSL) or Principal Medical Science Liaison (Principal MSL) to join our U.S. Medical Affairs organization and support the Southern U.S. territory.
The Senior/Principal MSL will serve as a field-based scientific and clinical expert, developing trusted relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), researchers, and other healthcare decision-makers. Through high-quality scientific exchange and collaboration, this role will advance understanding of rare diseases and Zevra's therapeutic portfolio, support evidence generation and clinical initiatives, and provide meaningful insights that help inform medical and clinical strategy.
The successful candidate will bring deep scientific expertise, strong business acumen, intellectual curiosity, and the ability to translate complex clinical information into meaningful scientific dialogue. They will maintain comprehensive knowledge of relevant disease states, Zevra's therapeutic portfolio, emerging science, the competitive landscape, and applicable regulatory and compliance requirements while ensuring all scientific exchange is accurate, balanced, and evidence-based.
This role is well suited for an experienced field-based Medical Affairs professional who is passionate about rare diseases, enjoys building meaningful relationships within the medical and scientific community, and thrives in a collaborative, growing organization focused on improving outcomes for patients with significant unmet needs.
Territory: S outheast/Southwest U.S. (FL, TX, GA, TN, LA, AL, MS, AR, NC, SC, CO, PR)
Zevra is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.