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Vitalief

IRB Coordinator Consultant (On-Site Livingston, NJ)

Vitalief, Livingston, New Jersey, us, 07039

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A healthcare consultancy is looking for an experienced IRB Coordinator Consultant to support a leading hospital research center. This role involves managing IRB activities, ensuring compliance with regulations, and providing guidance to researchers. Candidates should possess a Bachelor’s degree in a relevant field and have at least three years of experience in clinical research. Strong communication and organizational skills are essential, and proficiency in Microsoft Office is required. The position is based entirely on-site in Livingston, NJ, for a 6-month contract with potential extension. #J-18808-Ljbffr