Freelance Clinical Research Associate
IQVIAtaubaté, estado de são paulo, brHá 4 dias
Descrição da vagaConduct 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 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 Portuguese
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
Your Profile :
If you're ready to make an impact in clinical research, apply today!
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Clinical Research Associate • taubaté, estado de são paulo, br
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