Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II to join our dynamic FSP team. We have opportunities across the UK, particularly in London.
Fortrea is a global, innovative organization driving advancements in clinical research, and we are looking for a dedicated professional to ensure compliance with regulatory guidelines and company SOPs while working on diverse studies.
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 related 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.
* Strong communication, organizational, and problem‑solving skills.
* A valid driver’s license and willingness to travel.
We encourage applications from all backgrounds. Learn more about our EEO & Accommodations request here.
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