Freelance Regional Clinical Trial Manager (Remote)
52650
Posted: 16/07/2026
- Latvia, United Kingdom
- Contract
Would you like to join an exciting and collaborative role that encourages curiosity and supports professionals that want to do things differently? If so, this opportunity is for you, and will redefine what it means to work for a CRO
The Role
Location: Remote
You'll oversee clinical trial operations across multiple sites, owning the successful execution of trials while keeping timelines on track and standards high. You'll manage Clinical Trial Coordinators (CTCs), CRAs, and Business Partners assigned to your trials and report on regional progress and issues to the Therapeutic Area Lead at Clinical Project Review Meetings and to CTLs at Country Oversight Meetings. You'll keep the Clinical Trial Management System updated, join Investigator Meetings as needed, and organise them in your region when required. This is a 156-hour-per-month contract running to the end of 2026, with annual renewal. Start ASAP.
About You
Ready to Take the next step in your career?
If you're a driven clinical trials professional ready to make an impact I’d love to hear from you. Email me your CV or a time to speak at: archie.smith@barringtonjames.com
The Role
Location: Remote
You'll oversee clinical trial operations across multiple sites, owning the successful execution of trials while keeping timelines on track and standards high. You'll manage Clinical Trial Coordinators (CTCs), CRAs, and Business Partners assigned to your trials and report on regional progress and issues to the Therapeutic Area Lead at Clinical Project Review Meetings and to CTLs at Country Oversight Meetings. You'll keep the Clinical Trial Management System updated, join Investigator Meetings as needed, and organise them in your region when required. This is a 156-hour-per-month contract running to the end of 2026, with annual renewal. Start ASAP.
About You
- A degree in a related field (life sciences, nursing, or similar), with at least 5 years' experience in clinical trial management — CRO or pharmaceutical background preferred
- A track record of successfully managing regional or multi-site clinical trials
- Excellent written and verbal English, additional languages are a plus
- A collaborative mindset, grounded in honesty and trust
- Sharp problem-solving skills and the ability to adapt quickly when things shift
- Willingness to travel, with a valid driver's licence
Ready to Take the next step in your career?
If you're a driven clinical trials professional ready to make an impact I’d love to hear from you. Email me your CV or a time to speak at: archie.smith@barringtonjames.com
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