Medical Director, Clinical Development (Oncology)

Medical Director, Oncology Clinical Development Contract: Temporary - 6 months Location: Remote - UK (client based in London) Rate: (INSIDE IR35) - circa. £1125 per day (Umbrella)* SRG are seeking an experienced Clinical Development Medical Director with Oncology expertise to support a leading pharmaceutical company on a temporary basis. Join a team dedicated to advancing innovative oncology therapies through high quality clinical research. This is an exciting opportunity for a physician leader to shape clinical development strategy, drive global oncology trials, and collaborate with leading scientific experts. Key Responsibilities Lead the design, development, and execution of Phase I-III oncology clinical trials. Provide medical oversight and monitoring for ongoing studies, including safety and eligibility reviews. Contribute to clinical development strategies that support regulatory submissions and successful product launches. Interpret and communicate clinical study data, including efficacy, safety, and patient outcomes. Collaborate with cross-functional teams across clinical, regulatory, biostatistics, research, and medical affairs. Build and maintain strong relationships with external scientific leaders, investigators, and key opinion leaders.Skills & Experience Required MD (or equivalent) with board certification or eligibility in Medical Oncology, Hematology, Radiation Oncology, or Internal Medicine with relevant oncology experience. Experience in pharmaceutical, biotechnology, or clinical research environments. Strong understanding of the clinical drug development process and execution of clinical trials. Demonstrated experience reviewing and interpreting clinical data to inform development decisions. Knowledge of regulatory requirements and Good Clinical Practice (GCP). Strong scientific communication, stakeholder engagement, and cross-functional leadership skills.Preferred Qualifications Advanced degree such as PhD, MBA, or MPH. Experience leading oncology clinical development programmes and clinical trial strategy. Track record of scientific publications, research leadership, or recognised clinical expertise. Strong knowledge of evolving oncology treatment landscapes, clinical practice trends, and competitive developments.To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed) *PAYE also possible - please enquire for more information Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy