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The Clinical Research Associate is responsible for managing clinical study sites, conducting monitoring visits, and ensuring adherence to ICH GCP guidelines and sponsor protocols. They also safeguard data integrity through source document review and ensure sites remain audit-ready throughout the trial duration.
Main Responsibilities:
Qualifications (Minimum Required):
If you're looking to grow your career within a global organization while working in a collaborative FSP environment, we'd love to hear from you. At Fortrea, you'll have the opportunity to contribute to meaningful clinical research, work alongside industry-leading experts, and help bring innovative therapies to patients worldwide.
Apply today and join Fortrea's FSP team in Portugal, where your expertise can make a real difference in advancing healthcare!
Learn more about our EEO & Accommodations request here.
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