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: Full-time remote role with opportunities for professional growth and global impact.
- Other info: Exciting chance to influence global clinical trial strategies and operations.
- Why this job: Make a difference in cancer treatment while collaborating with top professionals worldwide.
- Qualifications: 6+ years in clinical research, strong project management skills, and oncology trial experience.
The predicted salary is between 60000 - 80000 € 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.
- 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.
- Maintain oversight of clinical trial site performance through monitoring report review and regular communication with investigators and study staff.
- Support development and tracking of clinical trial budgets and site-level financial management.
- Identify and proactively manage study risks and operational challenges.
Qualifications:
- 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).
- 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.
Opportunity to join a growing international biotech organisation. Work on innovative oncology therapies with global impact. 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 Trials Project Manager in High Wycombe employer: Barrington James
Join a dynamic and innovative biotechnology company that is at the forefront of developing groundbreaking therapies for cancer and other serious diseases. As a Clinical Trials Project Manager, you will thrive in a collaborative remote work environment that prioritises employee growth and offers significant exposure to global clinical trial strategy. With a strong commitment to compliance and quality, this role provides an exciting opportunity to make a meaningful impact in the field of oncology while enjoying the flexibility and support of a growing international team.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trials Project Manager in High Wycombe
✨Network Like a Pro
Get out there and connect with folks in the industry! Attend conferences, webinars, or local meetups related to clinical trials and oncology. You never know who might have a lead on your next big opportunity.
✨Showcase Your Experience
When you get the chance to chat with potential employers, make sure to highlight your relevant experience in clinical operations and project management. Share specific examples of how you've successfully managed trials and navigated challenges.
✨Be Ready for Interviews
Prepare for interviews by brushing up on your knowledge of ICH-GCP, FDA, and EU regulations. Be ready to discuss how you've applied these in your previous roles, especially in oncology trials. Confidence is key!
✨Apply Through Our Website
Don't forget to check out our website for job openings! Applying directly through us not only shows your interest but also gives you a better chance of landing that interview. Let's get you into that exciting role!
We think you need these skills to ace Clinical Trials Project Manager in High Wycombe
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Trials Project Manager role. Highlight your relevant experience in clinical operations, especially in oncology trials, and showcase any specific achievements that align with the job description.
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 makes you a perfect fit for our team. Don’t forget to mention your experience with CROs and project management.
Showcase Your Skills:In your application, be sure to highlight your understanding of ICH-GCP, FDA, and EU regulations. We want to see how your skills in budget management and risk identification can contribute to our innovative projects.
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 this exciting opportunity in our growing biotech company!
How to prepare for a job interview at Barrington James
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial phases, especially Phase I–II oncology trials. Familiarise yourself with ICH-GCP, FDA, and EU regulations, as these will likely come up in conversation.
✨Showcase Your Experience
Prepare to discuss your previous roles in clinical operations and project management. Highlight specific examples where you've successfully managed budgets, timelines, or CRO relationships, as this will demonstrate your capability for the role.
✨Be Ready for Scenario Questions
Expect questions that ask how you would handle specific challenges in clinical trials. Think about potential risks and operational challenges you’ve faced before, and be ready to explain how you navigated them.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s current projects, their approach to oncology trials, and how they collaborate with CROs. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.
