- Professional
Are you looking to grow your career in clinical research?
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.
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