Hiring.Camp

CRA II - SCRA - Scotland

Fortrea

·

Today

Location
Maidenhead, United Kingdom
Workplace
Remote
Type
Full-time
Experience
2+ years
Source
Workday

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.

Skills

GCPClinical TrialsCompliance

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