About this role
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.