CRA II - SCRA - Scotland

FTPOL Fortrea Poland Sp z o.o.

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Maidenhead Until 9/27/2026 2+ years exp First posted July 29, 2026 Last posted July 29, 2026
Job description

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 Scotland, where you'll work on a variety of clinical studies while developing your expertise in a supportive, collaborative environment.
 

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.
     

Key Responsibilities:

  • 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.
     

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 this role

Summary

Monitor clinical study sites, ensure protocol compliance, support safety and data integrity.

Job title

CRA II - SCRA

Experience level

2+ years

Minimum experience

2+ years exp

Industry

healthcare

Location requirements

Based in Maidenhead, UK, remote work not specified.

Salary

Not specified

Management role

No

Skills & keywords

Required skills

life sciencesclinical researchICH-GCPregulatory requirementscommunication

Preferred skills

None specified

Specializations

clinical researchclinical trialsGCP
Locations

Structured locations inferred from the posting.

Maidenhead SL6, UK

On-site City