Medical Director, Tisotumab Vedotin

Role Summary

This Medical Director role is within the Tisotumab Vedotin program. The successful candidate will support a late-stage clinical trial and ideally has prior experience in clinical trials and 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: Medical degree
• Required: 2-5 years industry experience
• Preferred: Board certified/eligible in oncology or equivalent