Is accountable for the medical & scientific integrity of the study and the wellbeing of the patients enrolled in one or more clinical trials
Applies technical and clinical/medical skills to ensure the design of efficient and high-quality clinical trials
Responsible for effective execution of studies and works in close partnership with other clinical and medical colleagues, clinical operations, and other functional lines
Accountable for timely delivery of a quality protocol, clinical execution of clinical trials
Responsible for providing clinical/medical input to SAP, TLFs and BDR
Serves as the primary contact with external investigators and internal study team for questions relating to clinical/medical aspects of protocol
Requirements
Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university and has Clinical Research experience
Been 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 space
Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management
Demonstrated clinical/medical, administrative, and project management capabilities, as well as excellent verbal and written communication skills in English
Benefits
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Paid personal days
Paid caregiver/parental leave
Paid medical leave
Health benefits including medical, prescription drug, dental, and vision coverage
Job title
Associate Director, Clinical Development – Medical Director, MD Required
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