IRB Coordinator
VitaliefNew Jersey, United States
Posted October 3, 2025
Full Time
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 to join their team in Livingston, NJ. The role supports a leading hospital research center, administering and overseeing IRB activities. The Coordinator will assist with research protocol review, grant activities, and ensure compliance with regulations, while also collaborating with investigators and IRB members.
Requirements
- Coordinate and manage all IRB activities.
- Review protocol submissions and recommend level of review.
- Draft and issue correspondence and regulate.
Benefits
- Competitive benefits
- Professional development opportunities
- Health insurance
- Disability insurance
- Retirement plan