Social network you want to login/join with:col-narrow-leftClient:EvidilyaLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:8662617666420211712337145Job Views:3Posted:27.08.2025Expiry Date:11.10.2025col-wideJob Description:Evidilya, the dedicated Contract Research Organization of Sprim Health Group, operates as a full-service international expertise in successfully developing and managing observational, pre-clinical, and clinical trials. We are looking for a:Clinical Research AssociateTo reinforce the Operational Italian Team.Main Responsibilities:Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close-out visits, according to SOPs and study Monitoring Plan.Write Monitoring Reports and manage site activities, including follow-up activities.Check data integrity.Support the team in submitting the study to ethics committees/IRBs.Hard & Soft Skills:Bachelor’s degree/MD or equivalent in a technical-scientific field.Proven experience in clinical monitoring and relevant training in the field.Proven GCP-ICH training.Current CRA certification as per MoH decree 15/11/2011.Excellent organizational and time management skills.Additional Requirements:Availability to travel, especially within Central-South Italy.What We Offer:Full remote work opportunity.Multicultural, young, and dynamic work environment.
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