Hybrid Clinical Research Monitor - Regulatory Data
Mass General Brigham Incorporated
Mass General Brigham Incorporated provides a hybrid role for a Site Monitor who conducts monitoring visits to ensure protocol and regulatory compliance with federal guidelines and accurate e-CRFs from source documents. Responsibilities include drafting monitoring plans, training staff at initiation, reviewing regulatory documents, maintaining site communications, and documenting findings. A Bachelor's degree and 1–2 years' clinical research experience are preferred. #J-18808-Ljbffr Mass General Brigham Incorporated
Vacancy posted 1 day ago
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