Project Coordinator – Biometrics Delivery

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

Job summary

A leading company is seeking a detail-oriented Project Coordinator – Biometrics Delivery to support key activities in clinical research. This fully remote role offers the opportunity for career progression into project management while also allowing candidates to contribute to impactful biometrics delivery efforts. Ideal applicants will have 2-3+ years of experience in clinical trials and strong organizational skills.

Benefits

Fully remote role

Long-term contract

Opportunity for career progression

Qualifications

• 2–3+ years of experience in the clinical trial process.
• Strong organisational and communication skills.
• Proficiency with project and data management tools.

Responsibilities

• Provide day-to-day administrative and operational support for biometrics delivery activities.
• Manage project documentation, trackers, and timelines.
• Coordinate with stakeholders and monitor clinical study metrics.

Skills

Organisational skills

Communication

Project management

Tools

Excel

SharePoint

Smartsheet

Power Applications

Job description

Social network you want to login/join with:

Project Coordinator – Biometrics Delivery, plymouth

col-narrow-left

Client:

Kelly Science, Engineering, Technology & Telecom

Location:

plymouth, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

col-wide

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.