Experienced Clinical Research Associate, Multi Sponsor

26 set - Provincia di Varese
Medpace

In this full-time role, you join Medpace’s Clinical Monitoring team to support site-based trials in Italy, helping advance clinical development for diverse therapies. You will perform monitoring visits, ensure protocol and regulatory compliance, and contribute to data integrity and site performance. The position offers comprehensive training and a clear path for professional growth within a global CRO. Your work will directly impact trial quality, patient safety, and timely study delivery.Flexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesConduct qualification, initiation, monitoring, and closeout visits per the approved protocolCoordinate with site staff including coordinators and physiciansVerify investigator qualifications, training, facilities, laboratories, equipment,



and staffPerform source data verification and ensure good documentation practices (GCP/SOPs) and report protocol deviationsConfirm eligibility of enrolled subjects and perform regulatory document reviewsOversee medical device and/or investigational product/drug accountability and inventoryReview adverse events and related data for accurate reportingAssess site recruitment and retention performance and suggest improvementsPrepare monitoring reports and follow-up letters with actionable recommendationsMaster in health-related fieldPrevious experience as CRAWillingness to travel 60-80% nationallyFamiliarity with Microsoft OfficeFluent in English and ItalianStrong communication and presentation skills would be considered a plusteam collaborationMicrosoft OfficeGood documentation practices (GCP)Regulatory document reviewExperienced Clinical Research Associate, Multi Sponsor varese, lombardia, it#J-18808-Ljbffr

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