Key skills
Project ManagementCommunication
About this role
Role Overview
- Accountable for the scientific integrity of the study
- Ensure design of efficient and high-quality clinical trials
- Provide clinical input to support development of the protocol design document
- Manage approval of Informed Consent Documents (ICDs)
- Review safety data and ensure TMF compliance
Requirements
- BA/BS or equivalent qualification with 6+ years of experience in biopharmaceutical industry in clinical research and development
- MBA or MS equivalent with 5+ years of experience
- Advanced Degree with 1+ years of experience
- Demonstrated clinical, administrative, and project management capabilities
- Excellent verbal and written communication skills in English
Benefits
- 401(k) plan with Pfizer Matching Contributions
- Pfizer Retirement Savings Contribution
- Paid vacation
- Paid holiday and personal days
- Paid caregiver/parental leave
- Paid medical leave
- Health benefits including medical, prescription drug, dental and vision coverage