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Fortrea

Clinical Research Associate II / Senior Clinical Research Associate

Clinical Research Associate II / Senior Clinical Research Associate

Posted 2 weeks ago

ScotlandRemote

Clinical Research Associate II / Senior Clinical Research Associate

Fortrea

Permanent
Full-Time
Sign up to unlock the estimation.Sign up to unlock the estimation~£40,000 - £55,000per annum· Meev estimate

Posted 2 weeks ago

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.

Fortrea is an equal opportunity employer. Learn more about EEO accommodations.
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Fortrea

A global CRO advancing clinical trials from Phase I to IV with tailored solutions

DurhamContract Research1000+
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Fortrea

Contract Research

Shape the future of medicine by working on trials that deliver treatments patients need. Collaborate across 90 countries with scientists, clinicians, and strategists driving innovation in clinical development every day.

Click to learn more
Fortrea logo

Fortrea

Contract Research

Shape the future of medicine by working on trials that deliver treatments patients need. Collaborate across 90 countries with scientists, clinicians, and strategists driving innovation in clinical development every day.

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