Experienced CRAs in Thatcham

Overview

Fortrea is hiring experienced CRAs (minimum of 2 years of independent monitoring experience) on different levels of seniority to join our client-dedicated team. This role is remote, offering an exciting opportunity 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

• Bachelor’s or Master’s degree in Life Sciences or equivalent.
• ≥ 3 years of relevant clinical research experience, with at least 2 years of previous monitoring experience.
• Ability to work independently and manage multiple priorities.
• Basic knowledge of regulatory guidelines and the clinical trial process.
• Strong communication, organizational, and problem-solving skills.
• Valid driver’s license and willingness to travel nationally (6-8 visits/month).

Ready to take the next step in your CRA career? Apply now and be part of groundbreaking clinical research at Fortrea!

Learn more about our EEO & Accommodations request here.