Vitalief
An experienced IRB Operations Manager will lead the day-to-day operations of a client's Human Subjects Protection Program (HSPP), overseeing regulatory compliance and workflow efficiency. The role involves supervising staff, managing IRB review pathways, and serving as a subject matter expert on human subjects research protections and federal regulations. Collaboration with researchers, compliance teams, and administrative stakeholders is essential to resolve issues and ensure high-quality service delivery.
Headquarters
New Brunswick, New Jersey, United States
Company Size
51-200 employees
Founded
2021
Vitalief is a clinical research operations consulting and managed services firm that helps academic medical centers, health systems, sponsors, CROs, and site networks improve the performance of their clinical research programs. They offer services spanning strategy and alignment, study start-up and activation, financial and revenue cycle operations, workforce and functional capacity, portfolio operations, and sponsor engagement. Vitalief differentiates itself by combining senior subject-matter expertise with AI-enabled infrastructure (VELARA) and a flexible engagement model that stays through delivery rather than exiting at a recommendation or placement.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Vitalief.
Vitalief didn’t post a salary, so this is our estimate from similar listings.
18% below the average for this role
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