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.
ROLE 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.
BASIC QUALIFICATIONS
- MD or DO with 3+ years of industry or clinical experience.
- Demonstrates a passion for helping patients with cancer and for the science of oncology.
- Has a collaborative style with internal company leadership and colleagues, as well as external collaborators, including investigators/medical professionals.
- Is a team player, works well in a team environment both as a leader and a key contributor.
PREFERRED QUALIFICATIONS
- Board certification in hematology/oncology preferred.
- Has a strong leadership presence and the ability to work effectively with other clinical and scientific leaders.
- Has a global perspective and mindset, with the ability to work effectively with colleagues from myriad cultures, backgrounds and geographies.
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