Description
We are seeking a CRA II/SCRA to join our dynamic FSP team at Fortrea. As a CRA II/SCRA, you will have the opportunity to work on diverse studies across the UK, particularly in the Midlands, while ensuring compliance with regulatory guidelines and company SOPs.
Why Join Fortrea?
- Be part of a global, innovative organisation 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).
- Basic knowledge of Regulatory Guidelines and the clinical trial process.
- Strong communication, organisational, and problem-solving skills.
- A valid driver’s license and willingness to travel.