Medical Director, Tisotumab Vedotin

Role Summary

This position is for a Medical Director within the Tisotumab Vedotin program. This position will be responsible for supporting a late-stage clinical trial. The successful candidate should ideally have prior experience in clinical trials and supporting development programs. Location: Hybrid.

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

Qualifications

• Required: 2-5 years industry experience
• Preferred: Board certified/eligible in oncology or equivalent

Education

• Medical degree