At a Glance
- 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.
- Other info: Fast-paced environment with significant exposure to global clinical trial strategies.
- Why this job: Make a real impact in the fight against cancer while collaborating with global teams.
- Qualifications: 6+ years in clinical research with strong project management skills.
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
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.
Clinical Project Manager in London employer: Barrington James
As a Quality Control Scientist in our leading pharmaceutical/biotech QC laboratory, you will thrive in a collaborative team environment that prioritises scientific excellence and compliance with GMP standards. We offer competitive day rates and the opportunity to enhance your skills in microbiology and quality control testing, ensuring your professional growth in a fast-paced and regulated setting.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager in London
✨Network Like a Pro
Get out there and connect with folks in the biotech scene! Attend industry events, webinars, or even local meetups. The more people you know, the better your chances of landing that Clinical Project Manager role.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience with oncology trials and project management. Share specific examples of how you've tackled challenges in past roles – it’ll make you stand out!
✨Be Ready for Interviews
Prepare for those interviews by brushing up on your knowledge of ICH-GCP and clinical trial regulations. Think about how you can demonstrate your organisational skills and ability to manage multiple trials effectively.
✨Apply Through Our Website
Don’t forget to check out our website for the latest job openings! Applying directly through us not only shows your interest but also gives you a better shot at getting noticed by our hiring team.
We think you need these skills to ace Clinical Project Manager in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Project Manager role. Highlight your relevant experience in clinical trials, especially in oncology, and showcase your project management skills. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your experience makes you a perfect fit for our team. Keep it concise but impactful – we love a good story!
Showcase Your Skills:Don’t forget to highlight your organisational and communication skills in your application. We’re looking for someone who can manage multiple trials and collaborate effectively with teams. Make sure these skills stand out!
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 don’t miss any important updates. Plus, we love seeing applications come in through our own platform!
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 clinical trial regulations. Being able to articulate your understanding of these guidelines will demonstrate your readiness to ensure compliance throughout the trial process, which is crucial for the role.
✨Engage with Cross-Functional Teams
Think about how you’ve collaborated with different teams in previous roles. Be prepared to share specific instances where your communication and stakeholder management skills made a difference in trial execution, as this is key in a collaborative biotech environment.
