Director of Oncology Studies
22 hours ago
We are seeking an experienced professional to lead our clinical trials in oncology. As a Clinical Study Manager, you will be responsible for overseeing the planning, design, initiation, progress, and conduct of clinical studies in Europe.
Key Responsibilities:
- Develop specific study aims and goals to support wider strategic, commercial, and technical objectives.
- Manage and organize all aspects of a clinical study from design and setup through close-out.
- Write and prepare study protocols, related subject information, and consent forms, as well as study/site-specific SOPs, case report forms, monitoring reports, and study reports.
Requirements:
- Bachelor's degree in nursing, biological sciences, or equivalent experience required.
- Proven experience in clinical research within a medical device, pharmaceutical, biotechnology, CRO, and/or healthcare setting.
- Extensive knowledge of clinical study and regulatory requirements.
Estimated Salary: £70,000 - £90,000 per annum based on location and experience.
Benefits: Opportunities for training and development, competitive benefits package, and flexible working arrangements.
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