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- Tasks: Manage and execute early-phase oncology clinical trials in a dynamic biotech environment.
- Company: Join a growing global biotechnology company focused on innovative cancer therapies.
- Benefits: Competitive salary, remote work, and opportunities for professional growth.
- Why this job: Make a real impact on global health by working on cutting-edge oncology treatments.
- Qualifications: 6+ years in clinical research with strong project management skills.
- Other info: Collaborative culture with significant exposure to international clinical trial strategies.
The predicted salary is between 36000 - 60000 £ per year.
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
- 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
- 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.
Clinical Project Manager in Coventry employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Project Manager in Coventry
✨Network Like a Pro
Get out there and connect with folks in the biotech scene! Attend industry events, webinars, or even local meetups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Show Off Your Skills
When you land that interview, make sure to highlight your experience with oncology trials and project management. Use specific examples to demonstrate how you've tackled challenges in past roles. We want to see how you can bring that expertise to our team!
✨Ask Smart Questions
During interviews, don’t just wait for them to ask you questions. Prepare some thoughtful ones about the company’s clinical trials and their approach to innovation. This shows you're genuinely interested and have done your homework!
✨Apply Through Our Website
We love seeing applications come through our website! It helps us keep track of candidates better. So, if you’re keen on joining our Clinical Operations team, make sure to submit your application directly through our site.
We think you need these skills to ace Clinical Project Manager in Coventry
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your clinical research experience, especially in oncology, and any project management roles you've held. We want to see how you fit into our fast-paced biotech environment!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how your background aligns with our mission at StudySmarter. Be sure to mention any relevant collaborations with CROs or your experience managing complex trials.
Showcase Your Achievements: When detailing your experience, focus on your achievements rather than just responsibilities. Did you improve trial timelines or manage a budget effectively? We love to see quantifiable results that demonstrate your impact in previous roles.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It helps us keep track of applications and ensures you’re considered for this exciting opportunity to join our Clinical Operations team!
How to prepare for a job interview at Barrington James
✨Know Your Trials
Make sure you’re well-versed in the specifics of oncology clinical trials, especially Phase I–II studies. Familiarise yourself with recent advancements in the field and be ready to discuss how your experience aligns with the company’s focus on innovative therapies.
✨Showcase Your Project Management Skills
Prepare examples that highlight your project management expertise, particularly in managing timelines, budgets, and vendor relationships. Be ready to discuss how you've successfully navigated challenges in past trials and what strategies you employed to keep everything on track.
✨Understand Regulatory Requirements
Brush up on ICH-GCP, FDA, and EU regulations relevant to clinical trials. Being able to articulate your understanding of these guidelines will demonstrate your readiness to ensure compliance and maintain high-quality standards throughout the trial process.
✨Engage with Cross-Functional Teams
Be prepared to discuss your experience collaborating with various teams, including CROs and internal stakeholders. Highlight specific instances where your communication and organisational skills helped facilitate smooth trial execution and fostered strong partnerships.