Clinical Trials Project Manager in Luton
Clinical Trials Project Manager

Clinical Trials Project Manager in Luton

Luton Full-Time 60000 - 80000 £ / year (est.) Home office possible
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Barrington James

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.
  • 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.
  • Other info: Exciting chance to influence global clinical trial strategies and operations.

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 Luton 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 a unique opportunity to make a meaningful impact on patient lives while working alongside passionate professionals in the field.
Barrington James

Contact Detail:

Barrington James Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trials Project Manager in Luton

✨Tip Number 1

Network like a pro! Reach out to your connections in the biotech and clinical trials space. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have a lead on that perfect Clinical Trials Project Manager role!

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of ICH-GCP and FDA regulations. Be ready to discuss your experience with Phase I–II oncology trials. Show them you’re not just a fit on paper but also in practice!

✨Tip Number 3

When you get an interview, think about how you can demonstrate your project management skills. Bring examples of how you've managed budgets and timelines in past roles. This will show you can handle the fast-paced environment they’re looking for.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search. Let’s get you that Clinical Trials Project Manager position!

We think you need these skills to ace Clinical Trials Project Manager in Luton

Clinical Trial Management
Project Management
Regulatory Compliance
Budget Management
Vendor Management
Risk Management
Oncology Clinical Trials
ICH-GCP Knowledge
FDA Regulations
EU Clinical Trial Regulations
TMF Management
Electronic Data Capture Systems
Cross-Functional Collaboration
Monitoring and Reporting

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 don’t forget to mention your understanding of ICH-GCP and regulatory requirements.

Craft a Compelling Cover Letter: Your cover letter should tell us why you’re the perfect fit for this role. Share specific examples of your past experiences managing clinical trials and how they align with our mission at StudySmarter. Keep it engaging and personal!

Showcase Your Project Management Skills: We want to see your project management prowess! Include details about how you've successfully managed timelines, budgets, and vendor relationships in previous roles. This will help us understand your ability to oversee CRO activities effectively.

Apply Through Our Website: Don’t forget to apply 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 you’re keen on joining our team at StudySmarter!

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.

Clinical Trials Project Manager in Luton
Barrington James
Location: Luton
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