Description
Milestone One is seeking a Site Coordinator to support a Clinical Study Site in clinical trial-related activities according to ICH-GCP and protocol requirements. The role involves acting as the primary liaison between sponsors/CROs and the site, assisting with scheduling monitoring visits, tracking patient enrollment, managing documentation, ensuring accurate data entry, resolving adverse events, handling investigational products, collecting regulatory documents, facilitating contracts, supporting investigator/site payments, performing study procedures, and preparing for audits. The ideal candidate will have a university degree in Life Sciences (preferably pharmacy, nursing, or lab analytics) and at least 2 years of experience as a site coordinator, demonstrating strong organizational, communication, and problem-solving skills in a fast-paced environment.
