Responsibilities: — Lead the set-up of each NHS Clinical Research Facility (CRF) site through to opening, including providing Local Information Packs and addressing site-specific queries. — Coordinate contracts with Trust R&D offices and uMed's contracts team. — Prepare each site to support bio-sample collections and clinical assessments by managing training, sample logistics, and equipment. — Manage day-to-day operations of the sites once open, acting as the main contact for site teams. — Facilitate Site Initiation Visits (SIV) and uMed platform site training. — Track visits and issues across all sites, provide weekly reports, and escalate risks early. — Align site capacity with uMed's patient recruitment to ensure referred participants are booked promptly. Requirements: — Minimum of 4 years of experience in clinical research site set-up. The role reports to the VP of Global Operations, is based in the UK, and is remote with an immediate start. The contract duration is 6 months. Sites are already identified and are required to facilitate bio-sample collection and clinical assessments, while uMed manages identification and recruitment.
Загружаем…