IRB Coordinator Consultant

Job Description

Job Description

About Vitalief

Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. Our team combines deep clinical research expertise with results-driven consulting to help organizations operate more efficiently and grow sustainably.

The Role

We are seeking an experienced IRB Coordinator Consultant to join the Vitalief team as a contractor.  In this role, you will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board (IRB) activities to ensure compliance with federal, state, and institutional regulations governing human subjects research. This role supports investigators, staff, and IRB members in the preparation, review, and approval of research protocols, while also assisting with Nussbaum grant activities.

Engagement Details

• Work Hours : 40 hours per week (8am to 4pm M-F)
• Work Location : 100% on-site in Livingston, NJ.
• Contract Duration : 6 months  (possible extension)
• Pay Rate : Market competitive (depends on experience level)

Responsibilities :

Qualifications :

PHYSICAL DEMANDS : Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.

IMPORTANT NOTE : Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

#LI-DNP

Powered by JazzHR

lfKp3BPFdR