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Clinical Research Associate
IQVIAOslo, Oslo, Norge3 days ago
Job descriptionConduct 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 3+ years CRA experience (incl. Phase I & oncology) Strong knowledge of clinical trial processes & GCP Excellent communication & organizational skills Ability to work independently and manage priorities Fluent in English and Norwegian
Join IQVIA Biotech as a Freelance CRA supporting Phase I–IV clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data, all while working with a passionate team in oncology research.
Freelance CRA – Oslo Area (Norway)
- Location : Oslo area preferred
- Hours : 24h / week (0.6 FTE)
- Start : ASAP
- Duration : 1 year
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Associate • Oslo, Oslo, Norge
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