Clinical Trial Manager
Location: United Kingdom (remote)
Industry: Biotechnology / Oncology / Haematology
Employment Type: Full-time
A growing global clinical-stage biotechnology company developing innovative therapies for cancer and other serious diseases is seeking a Clinical Trial Manager to join its Clinical Operations team in the UK.
This is an exciting opportunity to join a fast-paced, collaborative biotech environment where you will play a key role in the planning and execution of early-phase oncology clinical trials in partnership with global CROs and cross-functional internal teams.
The successful candidate will support the delivery of Phase I–II international studies, ensuring trials are conducted in compliance with regulatory requirements, timelines, and budget expectations.
Key Responsibilities
- Support the planning, implementation, and management of Phase I–II clinical trials in collaboration with CRO partners
- Oversee CRO and vendor activities, ensuring deliverables, timelines, and quality standards are maintained
- Contribute to the execution of clinical studies from protocol development through to final study report
- Coordinate preparation and review of key study documents including informed consent forms, case report forms, monitoring plans, and clinical reports
- Assist with vendor selection processes, including RFP development and CRO evaluation
- Maintain oversight of clinical trial site performance through monitoring report review and regular communication with investigators and study staff
- Track and manage study timelines, recruitment progress, and operational milestones
- Support development and tracking of clinical trial budgets and site-level financial management
- Ensure the Trial Master File (TMF) remains audit-ready throughout the lifecycle of each study
- Identify and proactively manage study risks and operational challenges
- Collaborate closely with cross-functional internal teams and external partners to ensure smooth trial execution
Requirements
- Bachelor’s or Master’s degree in life sciences, nursing, or a related discipline
- 6+ years of clinical research experience, including experience within a sponsor organisation or CRO
- Strong background in clinical operations and project management within biopharma
- Experience supporting oncology clinical trials (Phase I–III preferred)
- Experience working with CROs and external vendors
- Strong understanding of ICH-GCP, FDA, and EU clinical trial regulations
- Experience supporting clinical trial budgets and vendor management
- Knowledge of TMF management and electronic data capture systems
- Excellent organisational, communication, and stakeholder management skills
- Ability to manage multiple complex trials in a fast-paced environment
Why Apply
- Opportunity to join a growing international biotech organisation
- Work on innovative oncology therapies with global impact
- Highly collaborative and entrepreneurial environment
- Significant exposure to global clinical trial strategy and operations
If you are an experienced clinical operations professional looking to step into a highly visible role managing international oncology trials, we would welcome the opportunity to speak with you.
If you’d like, I can also give you a much stronger recruiter version of this ad (which will generate significantly more candidate responses on LinkedIn) — the structure above is good, but there are 3 changes that typically double applicant rates for CTM roles.
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