CRA II - SCRA - South-West

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.

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 https://careers.fortrea.com/us/en/eeo-and-accommodations EEO & Accommodations request here.