Clinical Research Associate

Barrington James is looking for a Clinical Research Associate

Job description

Overview

We are seeking a motivated and adaptable Clinical Research Associate II (CRA II) to join a growing clinical operations team within a collaborative and supportive environment. This role is ideal for an experienced CRA I looking to step into a CRA II position, an established CRA II, or a Senior CRA seeking the opportunity to work within a smaller, agile team structure.

The successful candidate will be responsible for monitoring clinical trial activities across multiple sites to ensure studies are conducted in compliance with protocol requirements, ICH-GCP guidelines, SOPs, and applicable regulatory requirements.

This position requires nationwide travel across the UK, with the potential for international travel in the future.


Key Responsibilities

  • Perform site selection, initiation, monitoring, and close-out visits in accordance with study timelines and monitoring plans
  • Build and maintain strong relationships with investigators and site staff
  • Ensure patient safety, data integrity, and protocol compliance throughout all study phases
  • Review source documentation and verify data entered into CRFs/eCRFs
  • Identify, document, and escalate site issues, protocol deviations, and risks appropriately
  • Support sites with study-related training and guidance
  • Prepare monitoring visit reports and follow-up documentation within required timelines
  • Collaborate cross-functionally with Clinical Operations, Project Management, Data Management, and other study teams
  • Participate in internal meetings, investigator meetings, and presentations as required
  • Maintain up-to-date knowledge of applicable regulations, SOPs, and industry best practice


Requirements

  • Previous experience working as a CRA within the pharmaceutical, CRO, or biotech industry
  • Suitable for:
  • Experienced CRA I candidates ready for progression
  • Existing CRA II professionals
  • Senior CRAs interested in a smaller team environment
  • Strong understanding of ICH-GCP and clinical trial processes
  • Excellent communication and presentation skills
  • Strong organisational and problem-solving abilities
  • Ability to work independently and manage multiple priorities effectively
  • Full willingness and ability to travel nationally on a regular basis
  • Ability to attend quarterly office meetings
  • Full UK driving licence preferred

Extra information

Status
Open
Education Level
Secondary School
Location
England
Type of Contract
Full-time jobs
Published at
24-05-2026
Profession type
Health / Medical
Full UK/EU driving license preferred
No
Car Preferred
No
Must be eligible to work in the EU
No
Cover Letter Required
No
Languages
English

Medical Jobs | Full-time jobs | Secondary School

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