Are you looking to grow your career in clinical research? Fortrea is hiring an experienced CRA to join our dynamic FSP team. We have opportunities across the UK, with a particular focus on the South West, offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.
Why Join Fortrea?
Be part of a global, innovative organization driving advancements in clinical research.
Work on cutting-edge trials across a range of therapeutic areas.
Enjoy flexible career progression, with opportunities at different CRA levels.
Benefit from a collaborative team environment that values mentorship and growth.
Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.
Manage all aspects of site activities, including site initiation, monitoring visits and closeouts.
Ensure patient safety, data integrity, and adherence to GCP guidelines.
Support feasibility assessments, investigator recruitment and vendor coordination.
Mentor junior team members and contribute to quality control efforts.
Track and report Serious Adverse Events (SAEs) as required.
University/college degree in life sciences or a relevant allied health field.
At least 2 years of experience in a related role (e.g., Site Management, CRA).
Basic knowledge of Regulatory Guidelines and the clinical trial process.
Strong communication, organizational, and problem-solving skills.
A valid driver’s license and willingness to travel.
Learn more about our EEO & Accommodations request here.
Skills Required
- University/college degree in life sciences or allied health field.
- At least 2 years of experience in a related role (Site Management, CRA).
- Basic knowledge of regulatory guidelines and the clinical trial process (including GCP).
- Strong communication, organizational, and problem-solving skills.
- Valid driver’s license and willingness to travel.
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
