other
Posted 4 weeks agoCRA II, London (client-dedicated)
at Fortrea
On-site
Responsibilities
- 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.
- Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.
Requirements
- Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II to join our dynamic FSP team.
- 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 .
Additional details
- We have opportunities across the UK, particularly in London , 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
- Strong communication, organizational, and problem-solving skills.
- A valid driver’s license and willingness to travel.
- Learn more about our EEO & Accommodations request here .