Experienced CRA - Norway

IQVIA · Oslo, Norway

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks an experienced Clinical Research Associate to conduct site monitoring, manage study progress, and ensure regulatory compliance across clinical trials in Norway. The role involves site visits, recruitment coordination, protocol training, and documentation management.

What they're looking for

Bachelor's degree in scientific or healthcare discipline preferred
Minimum 2 years of on-site monitoring experience
Proficiency in GCP and ICH guidelines
Strong knowledge of Microsoft Office suite and mobile devices
Fluent in English and Norwegian
Excellent organizational and problem-solving abilities

What you'll be doing

Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
Track subject recruitment plans and collaborate with sites on enrollment strategy
Administer protocol training and maintain regular communication with study sites
Evaluate site compliance with protocol, regulations, and escalate quality issues
Generate monitoring visit reports, follow-up documentation, and manage TMF/ISF files

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RoleLantern checkedNeeds clarity

Date posted16 days ago

Last source check1 day ago

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