CRA II/SCRA , 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.

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 .