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 months

 Your Role

Conduct 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 support

Your 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 Brazilian

If you're ready to make an impact in clinical research, apply today!

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com