Cra - South West - Fsp

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.   ### **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](https://careers.fortrea.com/us/en/eeo-and-accommodations).