Associate Medical Director providing medical/scientific expertise in safety evaluation and risk management of GSK assets. Ensuring patient safety while collaborating across teams in clinical development and post - marketing settings.
About the role
- Medical Director for Tisotumab Vedotin program managing late-stage clinical trials. Leading clinical study teams and collaborating across functions for strategic clinical development.
Responsibilities
- Lead clinical study teams and ensure appropriate medical monitoring for ongoing clinical studies
- Lead development and maintenance of clinical documents (e.g. protocols and amendments, investigator brochures, clinical study reports)
- Lead development of clinical study documents to be used in regulatory interactions and filings
- Develop manuscripts, abstracts and presentations for scientific meetings
- Evaluate safety, pharmacology, and efficacy data from ongoing and completed studies to inform clinical strategy
- Conduct literature reviews and prepare summaries to support clinical development strategies
- Support ongoing study activities and collaborate across functions for study level deliverables
Requirements
- Medical degree
- 2-5 years industry experience
- Board certified/eligible in oncology or equivalent preferred.
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 including medical, prescription drug, dental and vision coverage
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