Executive Medical Director leading clinical development and bridging research at GSK. Overseeing strategic initiatives in aging biology and managing cross - functional teams in drug development.
About the role
- Clinical Development Medical Director responsible for medical and scientific oversight in clinical trials at Pfizer. Managing clinical deliverables and ensuring the integrity of clinical data.
Responsibilities
- Provides medical monitoring on one or more clinical trials
- Provides timely, study-related medical information and guidance
- Conducts and documents periodic safety data review and ongoing clinical/medical data review
- May independently lead clinical execution of one or more studies
- Ensures development of Study Informed Consent Documents and responses to external stakeholder requests
- Provides clinical guidance to the development of the Statistical Analysis Plan
- Establishes and manages External Data Monitoring Committees and Adjudication Committees
Requirements
- Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university
- 4+ years of experience in biopharmaceutical industry in clinical research and development
- Licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period
- Clinical research experience in Phase 3/pivotal trial space, preferably with experience in study design, start-up, conduct, and close-out, including regulatory submissions and inspections
Benefits
- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation, holiday and personal days
- Paid caregiver/parental and medical leave
- Health benefits to include medical, prescription drug, dental and vision coverage
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