Project Coordinator – Biometrics Delivery

JR United Kingdom; High Wycombe; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading company in the field of clinical research is seeking a Project Coordinator – Biometrics Delivery, fully remote for UK-based candidates. This role involves supporting essential operations in clinical trials, focusing on documentation, process coordination, and collaboration with various teams. Ideal candidates will have experience in the clinical trial process, strong organisational skills, and are proactive in improving practices.

Benefits

Opportunity for career progression into project management

Fully remote role

Contribute to high-impact clinical research

Qualifications

• 2–3+ years of experience in the clinical trial process.
• Experience coordinating across multiple teams.
• Ability to work independently and manage competing priorities.

Responsibilities

• Provide day-to-day administrative and operational support for biometrics delivery activities.
• Manage and maintain project documentation, trackers, timelines, and communication tools.
• Track deliverables and milestones across multiple studies.

Skills

Organisational skills

Communication skills

Statistical programming

Data management

Tools

Excel

SharePoint

Smartsheet

Power Applications

Job description

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Project Coordinator – Biometrics Delivery, high wycombe

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Client:

Kelly Science, Engineering, Technology & Telecom

Location:

high wycombe, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

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Job Description:

Project Coordinator – Biometrics Delivery (Remote, UK-based)

Location: Remote (UK-based candidates only)

Employment Type: Seconded through our FSP Programs

We are seeking a detail-oriented and highly organised Project Coordinator – Biometrics Delivery to support key operational activities across clinical research programs. This role focuses on documentation, tracking, and process coordination related to biometrics deliverables, including statistical programming and biostatistics, in collaboration with supplier partners and internal study teams.

This is a fantastic opportunity for someone with experience in the clinical trial process who is looking to build a long-term career path, with the potential to progress into a project management role.

Key Responsibilities:

• Provide day-to-day administrative and operational support for biometrics delivery activities
• Manage and maintain project documentation, trackers, timelines, and communication tools
• Track deliverables and milestones across multiple studies to ensure progress and adherence to timelines
• Coordinate with cross-functional stakeholders to support alignment and efficient workflow
• Monitor and analyse metrics related to clinical studies, statistical programming, and biostatistics
• Support compliance with internal processes and external regulatory requirements
• Identify areas for process improvement and assist in implementation of best practices

Requirements:

• 2–3+ years of experience in the clinical trial process, with an understanding of statistical and programming deliverables and milestones
• Strong organisational and communication skills with experience coordinating across multiple teams
• Proficiency with Excel, SharePoint, Smartsheet, Power Applications, and other project and data management tools
• Familiarity with quality metrics, performance benchmarks, and regulatory compliance in clinical research
• Ability to work independently, manage competing priorities, and maintain accuracy in a fast-paced environment

What’s on Offer:

• Fully remote role for UK-based professionals
• Long-term contract with opportunity for career progression into project management
• A chance to contribute to high-impact clinical research and biometrics delivery efforts

If you're looking for a meaningful role that offers both responsibility and room to grow, we encourage you to apply.