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 Brazil
• Hours: 1 x 0.35 FTE and 1 x 0.6 FTE
• Start: ASAP
• Duration: 6 months

Your Role

• Conduct site evaluations, initiations, monitoring & close-outs
• Ensure GCP compliance and data integrity
• Collaborate with investigators and internal teams
• Review protocols, study manuals, and eCRFs
• Support site staff with training and issue resolution
• Track investigational product inventory and documentation
• Attend investigator meetings and study-related events
• Contribute to audit readiness and inspection support

Your Profile:

• 2+ years CRA including site monitoring experience
• IQVIA monitoring experience
• Strong knowledge of clinical trial processes & GCP
• Excellent communication & organizational skills
• Ability to work independently and manage priorities
• Fluent 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