Senior Medical Science Liaison - Central Territory
New
V
Valneva USABiopharmaceutical, Vaccines
Dallas, Georgia, United StatesFull-TimeSenior
Salary not disclosed
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Job Details
- Experience
- Five or more years of relevant experience; three or more years of field medical/MSL experience preferred.
- Required Skills
- Stakeholder management
Requirements
- Advanced degree in a relevant clinical or scientific discipline (MD, DO, PharmD, PhD, DNP, NP, PA, MPH) with substantial clinical/scientific experience.
- Five or more years of relevant experience in Medical Affairs, vaccines, infectious disease, clinical development, epidemiology, public health, or the biopharmaceutical industry.
- Three or more years of field medical/MSL experience preferred.
- Expertise in vaccines, infectious diseases, epidemiology, travel medicine, or immunization policy.
- Experience discussing clinical evidence, study design, endpoints, limitations, and safety data with sophisticated external experts.
- Demonstrated success managing complex scientific stakeholder networks.
- Strong ability to work autonomously, prioritize strategically, and operate effectively in a matrix organization.
- Exceptional scientific communication, presentation, and insight-generation capabilities.
- Ability and willingness to travel extensively throughout the Eastern U.S.
- Residence near a major airport is strongly preferred.
Responsibilities
- Lead the development and execution of a territory-specific medical strategy prioritizing scientific engagement, evidence needs, and stakeholder impact.
- Establish long-term peer-to-peer partnerships with infectious-disease physicians, travel-medicine specialists, vaccinologists, epidemiologists, and public-health professionals.
- Conduct proactive and responsive scientific exchange on disease epidemiology, preventive-vaccine science, clinical development, efficacy, and safety data.
- Synthesize and communicate external insights to inform medical strategy, evidence generation, and clinical development initiatives.
- Identify research opportunities, potential investigators, and qualified study sites to support clinical research execution.
- Support compliant medical education, advisory boards, and scientific congress engagement.
- Serve as an internal scientific resource on regional clinical-practice variation, stakeholder priorities, and public-health dynamics.
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