Offer summary

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, organizational, and problem-solving skills..

Key responsabilities:

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.

Mentor junior team members and contribute to quality control efforts.

Job description

Are you looking to grow your career in clinical research?
Fortrea is hiring CRAs II to join our dynamic team. We have opportunities based in South West, 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.