Medical Science Liaison / Senior Medical Science Liaison
New
K
Kyverna TherapeuticsBiopharmaceutical
Remote ideally based MI, OH, Western PA, Upstate NY, KYFull-TimeSenior
Salary not disclosed
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Job Details
- Experience
- MSL: Doctorate degree OR Master’s degree & 3 years of Medical Affairs experience. Senior MSL: Doctorate degree & 2 years of Medical Affairs experience OR Master’s degree & 6 years of Medical Affairs experience.
- Required Skills
- CRM
Requirements
- Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, NP, PA, or equivalent).
- MSL role: Doctorate degree OR Master’s degree with 3+ years of Medical Affairs experience.
- Senior MSL role: Doctorate degree with 2+ years of Medical Affairs experience OR Master’s degree with 6+ years of Medical Affairs experience.
- Prior experience in cell therapy, CAR-T, immunology, rheumatology, nephrology, neurology, or hematology/oncology.
- Strong understanding of clinical trial design, clinical development, and medical affairs functions.
- Experience engaging with academic medical centers and specialty treatment centers.
- Ability to interpret and communicate complex scientific and clinical information.
- Excellent presentation, communication, and interpersonal skills.
- Experience supporting pre-commercial or launch-stage biotechnology organizations.
- Knowledge of autoimmune disease treatment landscapes and cell therapy operational concepts.
- Willingness and ability to travel 50-70% within the assigned geography.
Responsibilities
- Identify, establish, and maintain high‑quality scientific relationships with KOLs, investigators, academic medical centers, and treatment centers.
- Serve as a trusted scientific partner by providing fair‑balanced, accurate, and compliant scientific exchange regarding disease states and Kyverna’s CAR‑T programs.
- Develop and execute geography‑specific Medical Affairs and KOL engagement plans aligned with therapeutic area objectives.
- Collaborate with Clinical Development and Clinical Operations to support trial site identification, investigator engagement, and trial awareness.
- Capture and communicate timely, high‑quality medical insights to internal stakeholders to inform clinical and development decision‑making.
- Provide scientific support at congresses, advisory boards, and medical education forums while responding compliantly to medical information requests.
- Ensure timely completion of CRM documentation, administrative tasks, and pharmacovigilance responsibilities.
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