Job Opportunities API

Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK, particularly in the Midlands , 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). • 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 .