Freelance Clinical Research Associate

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 :

• FTE and 1 x 0.6 FTEStart : ASAPDuration : 6 months Your RoleConduct site evaluations, initiations, monitoring & close-outsEnsure GCP compliance and data integrityCollaborate with investigators and internal teamsReview protocols, study manuals, and eCRFsSupport 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!