Company Overview

A privately backed, science driven biotechnology company advancing innovative oncology programmes is seeking an experienced physician leader to strengthen its clinical development and medical strategy capabilities. 

The organisation operates with a strong translational mindset and a clear focus on delivering differentiated therapies for patients with high unmet need.

Role Overview

This role requires a medically trained Urologist with oncology experience who has successfully transitioned into industry and can operate comfortably at the interface of clinical development, medical strategy, and cross functional leadership.

The successful candidate will provide medical oversight across oncology programmes, contributing to development strategy, protocol design, safety review, and external scientific engagement. The role combines strategic leadership with hands on medical input and close collaboration with clinical, regulatory, and scientific teams.

Key Responsibilities

• Provide medical leadership across oncology clinical development programmes
• Contribute to clinical development strategy across early and or mid stage assets
• Support protocol development, review, and execution from a medical perspective
• Provide ongoing medical monitoring and safety oversight for clinical trials
• Act as a key medical voice in cross functional discussions with Clinical Operations, Regulatory, Biometrics, and Translational teams
• Contribute to investigator engagement, advisory boards, and key scientific interactions
• Support regulatory interactions and preparation of clinical and medical content as required
• Ensure patient safety, scientific integrity, and regulatory compliance across programmes

Candidate Profile

• Medical degree with specialist training in Urology and demonstrated oncology experience
• Minimum of 5 years industry experience within biotech or pharmaceutical companies
• Proven exposure to clinical development and or medical affairs in oncology
• Experience working on early stage and or mid stage clinical programmes, including Phase I and Phase II studies
• Strong understanding of clinical trial design, endpoints, and oncology development pathways
• Exposure to translational or biomarker driven development
• Previous involvement in regulatory interactions, investigator meetings, advisory boards, or scientific exchange activities
• Experience operating effectively within small to mid sized biotechnology environments
• Strong communication skills with the ability to engage internal and external stakeholders

Application

This search is being conducted on a confidential basis. For an initial discussion or to express interest, please reach out directly.