Vice President, Clinical Development and Medical Affairs
Health Care Administrators Association® (HCAA) · Philadelphia, PA
FULL-TIME
Posted Oct 30, 2026
Job Description
Vice President, Medical to lead clinical strategy and medical affairs for a rare disease portfolio, including Friedreich’s ataxia.
Key Responsibilities
• Provide medical oversight for clinical development plans, trial design, and data interpretation with scientific rigor and strong patient safety standards.
• Partner cross-functionally with R&D, regulatory, and commercial teams to support end-to-end clinical execution.
• Develop and guide benefit–risk strategy and ensure medical integrity in decision-making.
• Lead KOL and investigator engagement and represent the organization in scientific and regulatory forums.
• Direct publication strategy and mentor clinical teams to strengthen capabilities and standards.
• Shape a high-integrity, mission-focused culture in a fast-paced biotech environment.
Qualifications & Skills
• Executive-level expertise in clinical development and medical affairs for rare diseases.
• Strong knowledge of trial design, clinical data interpretation, and patient safety/benefit–risk assessment.
• Proven ability to collaborate with regulatory and commercial partners and lead external scientific engagement.
• Leadership, mentorship, and strategic communication skills, including scientific/regulatory representation.
Key Responsibilities
• Provide medical oversight for clinical development plans, trial design, and data interpretation with scientific rigor and strong patient safety standards.
• Partner cross-functionally with R&D, regulatory, and commercial teams to support end-to-end clinical execution.
• Develop and guide benefit–risk strategy and ensure medical integrity in decision-making.
• Lead KOL and investigator engagement and represent the organization in scientific and regulatory forums.
• Direct publication strategy and mentor clinical teams to strengthen capabilities and standards.
• Shape a high-integrity, mission-focused culture in a fast-paced biotech environment.
Qualifications & Skills
• Executive-level expertise in clinical development and medical affairs for rare diseases.
• Strong knowledge of trial design, clinical data interpretation, and patient safety/benefit–risk assessment.
• Proven ability to collaborate with regulatory and commercial partners and lead external scientific engagement.
• Leadership, mentorship, and strategic communication skills, including scientific/regulatory representation.
Additional Details
- City
- Philadelphia
- State
- Pennsylvania
- Country
- US
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