Medical Director – Oncology Clinical Development
Location: Home-Based / Remote (UK / Europe)
Contract Type: 12-Month Contract (FSP Model – Outsourced to Pharma)
Overview
We are seeking an experienced Medical Director in Oncology Clinical Development to join a dynamic and innovative clinical development environment. This is a one-year, home-based remote contract opportunity operating within a Functional Service Provider (FSP) model, supporting a leading global pharmaceutical organization.
This role is ideal for a physician with strong oncology expertise who is passionate about advancing cutting-edge therapies and shaping clinical strategy from early to late-stage development.
Key Responsibilities
* Lead and contribute to the design and execution of Phase I–III oncology clinical trials within a complex global matrix environment
* Drive high-quality protocol development, aligned with overarching Clinical Development Plans
* Provide medical leadership across the end-to-end clinical trial lifecycle (concept through to final study report)
* Interpret and communicate clinical data, including efficacy, safety, PK/PD, and patient-reported outcomes
* Act as the medical lead for ongoing trials, including real-time medical monitoring and safety oversight
* Collaborate cross-functionally with Regulatory Affairs, Pharmacovigilance, Biostatistics, and Research teams
* Support regulatory submissions and responses to health authority queries
* Build and maintain strong relationships with Key External Experts and Principal Investigators
* Contribute to publications (abstracts, posters, manuscripts) and broader scientific exchange
* Serve as a core member of Clinical Matrix Teams and contribute to disease area and medical strategy discussions
Candidate Profile
Essential Requirements:
* MD (or equivalent) with specialization in Medical Oncology, Hematology, Radiation Oncology, or Internal Medicine (with oncology/hematology experience)
* Minimum 3+ years’ experience in the pharmaceutical/biotech industry or relevant clinical setting
* Strong understanding of the clinical drug development process, including hands-on clinical trial involvement
* Proven knowledge of GCP and regulatory requirements
* Demonstrated experience in clinical research and/or publications
Preferred Qualifications:
* MD with additional advanced degree (PhD, MBA, MPH, etc.)
* 5+ years’ experience in oncology clinical development
* Experience leading oncology trials, including study design, data interpretation, and strategy
* Deep understanding of disease biology, treatment landscapes, and evolving clinical guidelines
* Medical licensure (active or eligible) in relevant jurisdiction
Why Apply?
* Fully remote, home-based flexibility
* Opportunity to work on a high-impact oncology pipeline
* Exposure to innovative and transformational therapies
* Collaborative, science-driven environment with global stakeholders
* Flexible contract within a well-established FSP delivery model