pIn this role you support clinical trial activities and documentation to enable efficient study execution. You will work with cross-functional teams to manage trial records, site activation, and regulatory submissions, ensuring quality and timely delivery. You help maintain eTMF and ISFs, support risk-driven monitoring, and facilitate communications across sites. This position offers exposure to international trials and a path to grow in clinical research within a collaborative environment. /pulliCollaborative and inclusive environment /liliHands-on experience across site activation, regulatory documentation, and study management /liliContinuous learning and professional development /liliCareer progression opportunities /liliCompetitive compensation and benefits /liliCoordinate and complete assigned clinical trial activities per the study task matrix /liliReview country and investigator files; document findings in systems /liliSupport audit readiness by ensuring study files follow schedules and procedures /liliProcess and maintain documentation within the eTMF; resolve missing or incomplete items /liliAssist with ISFs, pharmacy binders,



and study supplies preparation /liliSupport translations and translation quality control as required /liliProvide administrative support for site activation and start-up activities /liliTrack regulatory documentation and assist with regulatory submissions /liliMaintain records of site communications, follow-ups, and survey responses /liliSupport RBM activities and study coordination across platforms (Activate, eTMF, etc) /liliAssist with scheduling internal/client meetings and distributing project communications /liliCollaborate with cross-functional teams to meet milestones and deadlines /liliCommunicate site-related issues and risks to clinical and project colleagues /liliHigh school/secondary diploma or equivalent /liliAdditional university-level education in life sciences or healthcare is an advantage /liliExperience is beneficial but candidates with the right knowledge and motivation may be considered /liliEquivalent combinations of education, training, and directly related experience may be considered /li /ulIn this role you support clinical trial activities and documentation to enable efficient study execution. You will work with cross-functiona… #J-18808-Ljbffr

📌 Clinical Trial Coordinator (Cusano Milanino)
🏢 Experteer Italy
📍 Cusano Milanino