Clinical Research Administration

Grant Administration

This service delivers end-to-end support for grant-funded trials, including grant writing, compliance management, and financial oversight from pre-award, post-award, to closeout.

For Sites, it streamlines access to research funding, ensures compliant use of grant resources, and minimizes administrative burden.

For Sponsors and CROs, it increases confidence in Site fiscal responsibility and ensures regulatory adherence for grant-supported studies.

Why Choose Vitalief

Sponsors, CROs, and Sites choose Vitalief’s Clinical Research Administration services because we provide experienced professionals and proven processes that streamline trial execution and reduce administrative burden. Our support ensures regulatory compliance, timely documentation, and seamless coordination, enabling research teams to stay focused on quality, enrollment, and outcomes.

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