ppIn 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.
/pulliFlexible work environment /liliCompetitive compensation and benefits package /liliCompetitive PTO packages /liliStructured career paths with opportunities for professional growth /liliCompany-sponsored employee appreciation events /liliEmployee health and wellness initiatives /liliConduct qualification, initiation, monitoring, and closeout visits per the approved protocol /liliCoordinate with site staff including coordinators and physicians /liliVerify investigator qualifications, training, facilities, laboratories, equipment,

and staff /liliPerform source data verification and ensure good documentation practices (GCP/SOPs) and report protocol deviations /liliConfirm eligibility of enrolled subjects and perform regulatory document reviews /liliOversee medical device and/or investigational product/drug accountability and inventory /liliReview adverse events and related data for accurate reporting /liliAssess site recruitment and retention performance and suggest improvements /liliPrepare monitoring reports and follow-up letters with actionable recommendations /liliMaster in health-related field /liliPrevious experience as CRA /liliWillingness to travel *****% nationally /liliFamiliarity with Microsoft Office /liliFluent in English and Italian /liliStrong communication and presentation skills would be considered a plus /liliteam collaboration /liliMicrosoft Office /liliGood documentation practices (GCP) /liliRegulatory document review /li /ulpExperienced Clinical Research Associate, Multi Sponsor varese, lombardia, it /p /p #J-*****-Ljbffr

Experienced Clinical Research Associate, Multi Sponsor

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