Clinical Research Associate
Pubblicato il 15-08-2026 - Cv-Library in Perugia
When our values align, there's no limit to what we can achieve.At Parexel, we all share the same goal Ha le carte in regola per avere successo? Le seguenti informazioni devono essere lette attentamente da tutti i candidati.
- to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special
- a deep conviction in what we do.Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will vantaggi a patient. We take our work personally, we do it with empathy and we're committed to making a difference.Parexel FSP is hiring for two experienced CRA's at either the CRA II or Senior CRA level to join one of a large Sponsor's in the EU. This role is responsible for the site management,
site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study executionSome specifics about this advertised roleEnsure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices.Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and quality deliverables are met.Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites.Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution.Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicableWho are ParexelParexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.We supported the trial