At a Glance
- Tasks: Lead innovative oncology clinical trials and shape development strategies.
- Company: Join a leading pharmaceutical company dedicated to advancing cancer therapies.
- Benefits: Competitive daily rate, remote work, and opportunity to influence global trials.
- Other info: Temporary role with potential for significant career advancement.
- Why this job: Make a real impact in oncology and collaborate with top scientific experts.
- Qualifications: MD with oncology expertise and experience in clinical research required.
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.
- 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.
- 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.
Medical Director, Clinical Development (Oncology) in London employer: Carbon 60
At Carbon 60, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to thrive. Located in Harlow, this hybrid role offers flexibility and the chance to engage with a dedicated Quality team, ensuring your contributions directly impact our commitment to quality excellence. With opportunities for professional growth and development, joining us means being part of a forward-thinking company that values your expertise and dedication.
