IRB Coordinator Consultant
VitaliefNew Jersey, United States
Posted October 3, 2025
Contract / Temporary
About the Company
Vitalief Inc. specializes in recruiting top talent for clinical trials, offering strategic partnerships to overcome workforce challenges. By investing in their team and delivering high-quality services, Vitalief ensures clients can adapt to the evolving needs of the industry, ultimately making a positive impact on patients' lives.
Job Description
Vitalief is seeking an experienced IRB Coordinator Consultant to support a leading hospital research center in Livingston, NJ. The role involves administering and overseeing IRB activities, preparing protocols, and assisting with grant submissions to ensure compliance with regulatory standards. The position requires 40 hours per week with a fixed 6-month contract.
Requirements
- Under the direction of the Director of Graduate Medical Education and Clinical Research
- Review protocol submissions for completeness and accuracy
- Draft and issue correspondence reflecting IRB deliberations
- Maintain compliance with OHRP, FDA, ICH/GCP, and institutional regulations
- Manage IRB databases and protocol documentation
- Assist with emergency use protocols and special meetings
- Schedule and support Institutional Research Committee meetings
- Collaborate with other system IRB Coordinators and departmental staff
- Stay current on regulatory and legislative developments