Freelance clinical research associate

Há 9 horas


Brasília, Brasil IQVIA Tempo inteiro

Join IQVIA Biotech as a Freelance CRA supporting Phase 2 and 3 clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.We currently have two projects in Brazil:Location: Brazil - travel required for both roles across BrazilHours: 1 x 0.35 FTE and 1 x 0.6 FTEStart: ASAPDuration: 6 monthsYour RoleConduct site evaluations, initiations, monitoring & close-outsEnsure GCP compliance and data integrityCollaborate with investigators and internal teamsReview protocols, study manuals, and e CRFsSupport site staff with training and issue resolutionTrack investigational product inventory and documentationAttend investigator meetings and study-related eventsContribute to audit readiness and inspection supportYour Profile:2+ years CRA including site monitoring experienceIQVIA monitoring experienceStrong knowledge of clinical trial processes & GCPExcellent communication & organizational skillsAbility to work independently and manage prioritiesFluent in English and PortugueseIf you're ready to make an impact in clinical research, apply today



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