CRA II, London (client-dedicated)

Fortrea is hiring a CRA II 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.

• →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).
• 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.