Clinical Director leading care delivery across clinician teams in a fast - growing virtual women's health care company. Combines clinical leadership with direct patient care in a hybrid role.
About the role
- Medical Director responsible for overseeing clinical trials for Tisotumab Vedotin. Ensuring compliance and collaborating across functions while leading regulatory document 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
- Health benefits to include medical, prescription drug, dental and vision coverage.
- 401(k) plan with Pfizer Matching Contributions.
- Additional Pfizer Retirement Savings Contribution.
- Paid vacation, holiday and personal days.
- Paid caregiver/parental and medical leave.
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