Fortrea is hiring an experienced CRA (CRA II-SCRA) to join our dynamic FSP team. We have opportunities across the UK, particularly in London for CRAs with Phase I patient-study experience, 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.
   

Key Responsibilities:

• 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.
   

Qualifications:

• 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).
• Phase I patient-study experience.
• 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.