About the 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
.