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- Tasks: Lead exciting clinical trials and manage vendor relationships for impactful studies.
- Company: Join Parexel, a leader in clinical research with a focus on innovation.
- Benefits: Enjoy remote work flexibility, competitive salary, and opportunities for professional growth.
- Why this job: Make a difference in healthcare while balancing your personal life.
- Qualifications: 5+ years in clinical research with CRO oversight experience required.
- Other info: Dynamic role with the chance to shape global clinical trial strategies.
The predicted salary is between 48000 - 72000 £ per year.
Parexel is currently seeking a UK Clinical Trial Manager (CTM) to join us at short notice (to start in March 2026), dedicated to a single sponsor. The Clinical Trial Manager is responsible for the execution of study-level activities including but not limited to creating and updating trial-specific documents, vendor oversight & delivery, compound training and country and regional oversight of CRO operational delivery. This includes alignment on the feasibility strategy, target setting, risk reviews, and country challenges that could impact overall study delivery. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Responsibilities
- Manage integration of project team activities
- Manage strategic study operations including but not limited to study sites and tracking systems for regulatory submissions, drug supply and use, enrollment of subjects, regulatory document flow, study timelines, budget and financial information, performance metrics, and data flow
- Provide input on trial level operational strategies for clinical trials from protocol design to the final clinical study report for specific studies
- Provide input into global subject/patient recruitment plans
- Manage aspects of CRO/vendor identification and the day-to-day operational management activities of CROs and other vendors including set up, statement of work creation, and budget oversight
Qualifications
- Bachelor’s, nursing degree or equivalent required, science preferred.
- Minimum 5+ years of clinical research experience gained with a CRO, biotech or pharmaceutical company working on phase I-IV global clinical trials
- 2-3 years leading aspects of clinical trials
- CRO oversight experience is essential
UK Clinical Trial Manager - CRO Oversight - FSP - Remote employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land UK Clinical Trial Manager - CRO Oversight - FSP - Remote
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with CROs. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by diving deep into the company’s recent projects and challenges. Show us that you’re not just another candidate; you’re genuinely interested in how you can contribute to their success.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at Parexel.
We think you need these skills to ace UK Clinical Trial Manager - CRO Oversight - FSP - Remote
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Manager role. Highlight your relevant experience in clinical research, especially any CRO oversight you've done. We want to see how your background aligns with the responsibilities listed in the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention specific projects or experiences that relate to managing study operations and vendor oversight. We love seeing your passion for clinical trials!
Showcase Your Achievements: When detailing your experience, focus on your achievements rather than just duties. Use metrics where possible to demonstrate your impact, like successful patient recruitment rates or budget management. This helps us see the value you can bring to our team.
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 Parexel!
How to prepare for a job interview at Parexel International
✨Know Your Stuff
Make sure you’re well-versed in clinical trial management and the specific responsibilities outlined in the job description. Brush up on your knowledge of CRO oversight, vendor management, and regulatory submissions. This will not only help you answer questions confidently but also show that you're genuinely interested in the role.
✨Showcase Your Experience
Prepare to discuss your previous experiences in clinical research, especially any roles where you managed study operations or led aspects of clinical trials. Use the STAR method (Situation, Task, Action, Result) to structure your answers, highlighting how your contributions made a difference in past projects.
✨Ask Smart Questions
Interviews are a two-way street, so come prepared with insightful questions about the company’s approach to clinical trials, their challenges, and how they measure success. This shows that you’re not just looking for any job, but that you’re specifically interested in how you can contribute to their goals.
✨Be Yourself
While it’s important to be professional, don’t forget to let your personality shine through. The interviewers want to see if you’ll fit into their team culture. Share your passion for clinical research and how you balance work with your outside life, as this aligns with the company’s values.
