Global Study Start-Up Specialist
Fortrea
Fortrea is seeking a regulatory submission-focused professional to coordinate site activations and study maintenance. You will collect essential documents, adapt informed consent materials country-specifically, and liaise with regulators to ensure timely approvals. You will collaborate with senior staff to prepare submissions for IRB/IEC and other regulatory bodies, maintain audit-ready records, and support CTIS activities and vendor governance as needed. #J-18808-Ljbffr Fortrea
Vacancy posted 1 day ago
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