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Freelance CRA - Norway
IQVIAOslo, Oslo, Norge22 timer siden
JobbeskrivelseConduct 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
Overview
Join IQVIA Biotech as a Freelance CRA - Norway role. You’ll support Phase I–IV clinical trials, lead site visits, monitor compliance, and ensure high-quality data—working with a passionate team in oncology research.
Position details
- Location : Oslo area preferred
- Hours : ~24h / week (0.6 FTE)
- Start : ASAP
- Duration : ~1 year
Your role
Your profile
If you’re ready to make an impact in clinical research, apply today!
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
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Norway • Oslo, Oslo, Norge
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