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Conduct study site monitoring visits to ensure compliance with protocols, GCP, and regulatory requirements. Manage the full site lifecycle from initiation to closeout while supporting patient safety and data integrity.
Are you looking to take the next step in your clinical research career? Fortrea is seeking a CRA II to join our growing FSP team. This is a fantastic opportunity for candidates based in Scotland, where you'll work on a variety of clinical studies while developing your expertise in a supportive, collaborative environment.
Why Join Fortrea?
Key Responsibilities:
What We're Looking For:
At Fortrea, you'll have the opportunity to make a meaningful impact on patients' lives while continuing to grow your clinical research career alongside experienced and passionate professionals. We would love to hear from you!
Learn more about our EEO & Accommodations request here.
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