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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: Remote work, competitive salary, and the chance to make a global impact.
- Why this job: Be at the forefront of groundbreaking cancer research and collaborate with top professionals.
- Qualifications: 6+ years in clinical research with strong project management skills.
- Other info: Fast-paced, collaborative culture with significant career growth opportunities.
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.
Locations
Clinical Project Manager in Hampshire, Portsmouth employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Project Manager in Hampshire, Portsmouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech field, especially those who work in clinical operations. A friendly chat can lead to insider info about job openings or even referrals that could give you an edge.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and FDA regulations. We all know that confidence is key, so practice answering common interview questions related to clinical trial management to showcase your expertise.
✨Tip Number 3
Showcase your project management skills! Be ready to discuss specific examples of how you've successfully managed timelines and budgets in past trials. This will demonstrate your ability to handle the complexities of Phase I–II studies.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team and contributing to innovative oncology therapies.
We think you need these skills to ace Clinical Project Manager in Hampshire, Portsmouth
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 your experience with CROs and managing budgets, as these are key for us.
Showcase Your Achievements: When detailing your past roles, focus on your achievements rather than just responsibilities. Did you improve timelines or enhance trial quality? We love to see quantifiable results that demonstrate your impact in previous positions.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Barrington James
✨Know Your Trials
Before the interview, dive deep into 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
Be prepared to share concrete examples of how you've successfully managed multiple complex trials. Highlight your organisational skills and ability to meet tight deadlines, as these are crucial for the role of a Clinical Project Manager.
✨Understand Regulatory Requirements
Brush up on ICH-GCP, FDA, and EU clinical trial regulations. Being able to articulate your understanding of these guidelines will demonstrate your readiness to ensure compliance throughout the trial process.
✨Engage with Stakeholders
Think about how you’ve collaborated with CROs and internal teams in the past. Prepare to discuss your communication strategies and how you’ve effectively managed relationships to ensure smooth trial execution.