Responsible for medical and scientific oversight of clinical trials in Internal Medicine
Provides timely, study-related medical information and guidance
Conducts and documents periodic safety data review and ongoing clinical/medical data review
Represents the study team in internal protocol review governance submissions and interactions
Develops site selection criteria and ensures protocol training is delivered to site-facing colleagues
Ensures TMF compliance for clinical documents
Develops clinical guidance and reviews safety data

Primary medical degree (e.g., MD, DO, MBBS, MBChB)
4+ years of experience in biopharmaceutical industry in clinical research and development
Licensed by a licensing body to prescribe medicines for at least 2 years post intern/house officer/foundation period
Cardiometabolic disease experience preferred
Clinical research experience in study design, start-up, conduct, and close-out, including regulatory submissions and inspections
Scientific productivity via publications, posters, abstracts, and/or presentations
Extensive knowledge of clinical development, global and regional regulation, and ICH/GCP

401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Paid holiday
Paid personal days
Paid caregiver/parental leave
Paid medical leave
Health benefits including medical, prescription drug, dental, and vision coverage

Clinical Development Medical Director, MD Required

Key skills