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CRA II/SCRA , London (client-dedicated)
Fortrea · Maidenhead
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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. 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 .