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CRA II - SCRA

On-site in Maidenhead·Full-time·Added 1 month ago (last checked 4 Oct)

Fortrea

39 open roles

Overview

Job details

  • Full-time

    Per the ad.

Requirements

  • Work on-site in Maidenhead

    No relocation package mentioned.

  • Have 2+ years of experience

    Mid-level role.

Skills

Nice to have

The role

Are you looking to take the next step in your clinical research career? Fortrea is seeking an experienced CRA II or a SCRA1 to join our growing FSP team.

This is a fantastic opportunity for candidates based in the South-West region (Bristol/Bath/Swindon/Gloucester/Cheltenham/Cardiff/Exeter area), where you'll work on a variety of clinical studies while developing your expertise in a supportive, collaborative environment.

What you'll do

  • Conduct study site monitoring visits to ensure compliance with protocols, GCP, regulatory requirements, and company SOPs.
  • Manage all aspects of site activities, including site initiation, routine monitoring, and closeout visits.
  • Support patient safety, data integrity, and overall study quality.
  • Contribute to feasibility assessments, investigator engagement, and vendor coordination activities.
  • Build strong relationships with study sites and act as a trusted partner throughout the clinical trial lifecycle.
  • Track and report Serious Adverse Events (SAEs) as required.
  • Support less experienced team members and contribute to continuous quality improvement initiatives.

Why Join Fortrea?

  • Be part of a global, innovative organization helping to advance healthcare and improve patient outcomes.
  • Gain exposure to a diverse portfolio of clinical trials across multiple therapeutic areas.
  • Enjoy ongoing career development and opportunities for progression within our CRA community.
  • Join a supportive team culture that values collaboration, mentorship, and professional growth.
  • Benefit from the flexibility and stability of working within a strong FSP partnership.

What We're Looking For

  • Degree in Life Sciences or a related healthcare/scientific discipline.
  • Minimum 2 years of experience in clinical research, such as a CRA or Site Management role.
  • Good understanding of ICH-GCP, regulatory requirements, and clinical trial processes.
  • Strong communication, relationship-building, and organizational skills.
  • A proactive approach to problem-solving and managing priorities.
  • A valid driver's licence and willingness to travel to investigator sites as required.

At Fortrea, you'll have the opportunity to make a meaningful impact on patients' lives while continuing to grow your clinical research career alongside experienced and passionate professionals. We would love to hear from you!

Learn more about our EEO & Accommodations request here.

About Fortrea

Industry
Clinical Research
All open roles at Fortrea
Remote, the UK
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