Medical Director, Clinical Development, Specialty Medicine
Responsibilities:
- Act as medical expert and leader in interactions with external stakeholders
- Define clinical trial-related Clinical Development Program (CDP) goals and objectives
- Work closely with discovery teams to provide input on next-generation targets
- Ensure the relevance and accuracy of medical science underpinning clinical study concepts (CSC) via scientific review and consultation with internal/external experts
- Review and finalize clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings
- Lead the Global Clinical Study Team to deliver high-quality program deliverables on schedule
- Oversee medical content of clinical study reports, analysis of clinical data (including safety monitoring), and activities/procedures that ensure patient safety
Qualifications:
- M.D. or equivalent with board eligibility or board certification in Pulmonary/Critical Care or Cardiology (relevant experience acceptable)
- At least 2 years pharmaceutical industry experience (academic research considered)
- Experience in cardiovascular disease drug development (strongly preferred)
- Previous interactions with regulatory agencies or CTD (βdossierβ) submission in an ICH region (advantage)
Required/Preferred Skills:
- Clinical scientific knowledge applicable to clinical research
- Physician-scientist leadership and role-modeling for the team
Benefits:
- Comprehensive benefits (varies by location), including in the U.S.: health and wellness programs (medical, dental, vision, life, disability), fitness centers, 401(k) match, equity awards, annual bonuses, paid time off, paid leaves (e.g., military and parental leave)
Application Instructions:
- Apply now to take your first step towards living the Regeneron Way.