Vitalief’s Site Identification, Selection, Activation, and Ongoing Support services give Sponsors and CROs a complete solution to accelerate trial start-up and sustain consistent execution across all sites, regardless of phase, indication, or therapeutic area. Our specialized team of seasoned site experts serves as the central point of communication and coordination, managing every step from feasibility through trial execution. This includes site identification and qualification, oversight of the selection process, regulatory and IRB submissions/approvals, budget negotiations, contract execution, pharmacy preparation, and protocol-specific training. We also schedule and conduct Site Initiation Visits, ensuring every site receives consistent guidance, messaging, and compliance oversight.

But activation is only the beginning. Our ongoing site support keeps sites engaged and equipped throughout the trial lifecycle. We provide proactive communication, operational oversight, and troubleshooting to minimize disruptions, reduce mid-trial risks, and keep enrollment on track. By maintaining alignment between Sponsors, CROs, and Sites, we ensure that studies stay compliant, efficient, and milestone-ready.