Medical Director

A growing, discovery-driven biotechnology company is seeking an experienced Medical Director with expertise in gynecologic oncology, to join its Clinical Development team. This is a unique opportunity to play a key strategic and scientific role in advancing a cutting-edge gynecologic oncology pipeline.

The Medical Director will work closely with clinical, translational, and operational leaders to shape clinical strategy, drive early-phase trial execution, and ensure high-quality medical oversight across gynecologic oncology programs. This is a highly collaborative, cross-functional role suited to someone who thrives in an innovative, agile biotech environment.

• Contribute to the design, implementation, and execution of early-phase gynecologic oncology clinical trials.
• Provide medical and scientific oversight for clinical programs, partnering closely with external investigators, CROs, and internal clinical operations.
• Support the development of clinical strategy, protocol design, and study documents (IB, CSR, SAP, etc.) gynecologic oncology indications.
• Review and interpret clinical data, safety signals, and emerging efficacy results to inform program and portfolio decision-making.
• Partner with translational and research teams to integrate disease-relevant biomarker strategies and mechanistic insights.
• Represent Clinical Development in internal reviews, governance forums, and cross-functional planning discussions.
• Contribute to regulatory interactions and documentation supporting global submissions.
• Provide scientific and medical input into publications, presentations, and external collaborations within the gynecologic oncology community.

• MD with formal training and clinical expertise in gynecologic oncology, medical oncology or a closely related specialty.
• Experience in early clinical development within biotech or pharmaceutical settings, ideally in solid tumors or gynecologic malignancies.
• Demonstrated strength in clinical trial design, safety oversight, and data interpretation in early-phase studies.
• Proven ability to operate effectively in small, fast-moving, cross-functional teams.
• Strong communication skills, with credibility when engaging investigators, KOLs, and internal stakeholders.
• Comfortable working in a dynamic environment where priorities evolve as data emerge.

If you are interested in learning more, please send your updated resume to