Project Coordinator – Biometrics Delivery

JR United Kingdom; Bedford; Remote; GBP 30,000 - 45,000; Full time

Job summary

JR United Kingdom is seeking a Project Coordinator for Biometrics Delivery, focusing on project coordination and documentation for clinical research programs. This fully remote role requires 2–3 years of clinical trial experience and offers a long-term contract with growth potential into project management.

Benefits

Fully remote role for UK-based professionals

Long-term contract with career progression

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 in a fast-paced environment.

Responsibilities

• Provide day-to-day administrative and operational support for biometrics delivery activities.
• Manage and maintain project documentation and trackers.
• Coordinate with cross-functional stakeholders to support alignment.

Skills

Strong organisational skills

Communication skills

Statistical programming understanding

Tools

Excel

SharePoint

Smartsheet

Power Applications

Job description

Client:

Kelly Science, Engineering, Technology & Telecom

Location:

bedford, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

7

Posted:

26.06.2025

Expiry Date:

10.08.2025

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.

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Created on 26/06/2025 by JR United Kingdom