Clinical Trial Coordinator

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7cprnn

In 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.Collaborative and inclusive environmentHands-on experience across site activation, regulatory documentation, and study managementContinuous learning and professional developmentCareer progression opportunitiesCompetitive compensation and benefitsCoordinate and complete assigned clinical trial activities per the study task matrixReview country and investigator files; document findings in systemsSupport audit readiness by ensuring study files follow schedules and proceduresProcess and maintain documentation within the eTMF; resolve missing or incomplete itemsAssist with ISFs, pharmacy binders,



and study supplies preparationSupport translations and translation quality control as requiredProvide administrative support for site activation and start-up activitiesTrack regulatory documentation and assist with regulatory submissionsMaintain records of site communications, follow-ups, and survey responsesSupport RBM activities and study coordination across platforms (Activate, eTMF, etc)Assist with scheduling internal/client meetings and distributing project communicationsCollaborate with cross-functional teams to meet milestones and deadlinesCommunicate site-related issues and risks to clinical and project colleaguesHigh school/secondary diploma or equivalentAdditional university-level education in life sciences or healthcare is an advantageExperience is beneficial but candidates with the right knowledge and motivation may be consideredEquivalent combinations of education, training, and directly related experience may be consideredIn this role you support clinical trial activities and documentation to enable efficient study execution. You will work with cross-functiona…#J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7cprnn