Medical Science Liaison – Upper Midwest
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Job Description
Regional Medical Science Liaison responsible for executing clinical programs and fostering relationships within the medical community. Leading scientific communication and insights collection across therapeutic areas.
Responsibilities:
- As a Regional Medical Science Liaison, you will drive clinical program execution, foster connections with the medical community, communicate scientific and clinical information, and collect insights to inform strategic objectives.
- Serve as the primary interface with clinical trial sites, collaborating with Clinical Development and Operations to ensure high-quality study execution, specifically clinical trial enrollment.
- Participate in planning and setup for your region, aligning with local colleagues and CROs.
- Develop deep expertise in multiple therapeutic areas, including inflammatory bowel disease.
- Act as the regional subject matter expert and credible scientific leader.
- Build and maintain relationships with opinion leaders, clinical investigators, and study staff within your region.
- Provide scientific support to Clinical Development, Medical Affairs, Commercial, and other teams.
- Support activities such as local, regional, national, and as needed, international, congresses, share clinical and scientific insights with cross-functional teams.
- Operate ethically and comply with all laws, regulations, and policies.
Requirements:
- Minimum master’s degree with medical credential (NP, RN, PA) from an accredited institution
- Terminal degree (PharmD, PhD) highly preferred
- MSL with pharmaceutical experience and medical credential (RN) may be considered with bachelor’s degree
- MSL experience required (minimum 2-3 years)
- Drug pre-approval (pre-PDUFA) MSL experience required
- IBD/GI or immunology experience strongly preferred
- Strong written and verbal communication skills; ability to present medical/scientific information clearly
- Relationship-building and networking skills
- Excellent organization and results orientation
- Influence and negotiation skills
- Ability to work independently and in teams in a dynamic environment
- Experience with clinical trial design, conduct, and evaluation
- Permanent residence within assigned region
- Ability to travel 70% of the time
- Preference will be given to candidates residing near a major airport, ideally in an eastern half of the US or southeast location; residency in Texas or Florida is advantageous.
- Proficiency with Microsoft Suite and digital meeting platforms
- Safe driving record and valid driver’s license required
- Successful completion of Amplity and client training.
Benefits:
- Competitive base salary and bonus potential
- Generous PTO and paid holidays
- 401K, medical, dental, vision coverage
- Company-funded wellness program, long term/ short term disability, life insurance
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