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Fortrea
Overview
The role involves managing all aspects of clinical site monitoring, including initiation, routine visits, and close-out for oncology trials. Key duties include ensuring patient safety, verifying informed consent, and maintaining data integrity through CRF review and SAE reporting.
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Compensation
Salary not listed
Posted
9 days ago
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management. Ensures the protection of study patients and the integrity of data submitted on Case Report Forms.
1 month ago
