Director, Medical Science Liaison, Carolinas
Celcuity
Full-time
Remote friendly (Minneapolis, MN)
United States
$230,000 - $275,000 USD yearly
Medical Affairs
Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.
Role Summary
Director, Medical Science Liaison responsible for scientific exchange with HCPs and key decision makers on Celcuity’s products and disease states, supporting clinical trials. Travel within the territory and the US for medical conferences is expected.
Responsibilities
- Identify and cultivate professional relationships KOLs in designated tumor types.
- Maintain cross-functional field partnerships with field commercial teams and Clinical Development associates.
- Develop and expand synergistic relationships with KOLs for research, advisory, and educational partnerships.
- Assist the Clinical Development Team in identifying and educating potential clinical trial sites and troubleshoot issues during clinical trial conduct.
- Develop scientific expertise on Celcuity’s products, related disease states, and clinical practice in the therapeutic area.
- Communicate scientific content related to Celcuity’s products and disease states in written and verbal form.
- Follow all applicable laws, SOPs and guidance documents to ensure compliance.
- Provide scientific training to internal colleagues.
- Participate in Medical, Legal, and Regulatory review as needed in the role of scientific expert.
- Identify, categorize, and communicate key clinical insights related to the assigned disease state and products.
- Other duties as assigned.
Qualifications
- MD, PharmD, or PhD in Life Sciences, D.Sc., D.N.P, or D.O. degree
- Solid tumor oncology experience
- Excellent presentation and communication skills
- Ability to convey complex scientific concepts to diverse audiences
- 3+ years of related pharmaceutical Medical Science Liaison experience
- Breast Cancer experience
- Knowledge of clinical research design and GCP in oncology
- Experience at a small/start-up biopharmaceutical company
- Strong business acumen
- Experience with payor groups, market access, formulary committees, and treatment guidelines
- Experience managing territory resources and budgets; self-starter
- Experience launching products
Skills
- Presentation and communication
- Scientific writing and education
- Strategic stakeholder engagement
- Clinical trial site identification and support
- Regulatory and compliance awareness
Education
- MD, PharmD, or PhD in Life Sciences, D.Sc., D.N.P, or D.O. degree
Additional Requirements
- Travel within the territory and to US medical conferences