Experienced CRA - Sweden

IQVIA · Stockholm, Sweden

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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 and management activities for clinical trials in Sweden. The role ensures protocol compliance, data quality, and regulatory adherence across assigned study sites.

What they're looking for

Bachelor's degree in scientific or healthcare discipline
Minimum 2 years of on-site clinical trial monitoring experience
Strong knowledge of GCP and ICH regulatory guidelines
Proficiency with Microsoft Office (Word, Excel, PowerPoint)
Fluent written and verbal English communication
Strong organizational and problem-solving abilities
Ability to build effective professional relationships

What you'll be doing

Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
Support subject recruitment planning and track enrollment progress against project targets
Provide protocol training to sites and maintain regular communication regarding expectations
Evaluate site compliance with protocol requirements and escalate quality or regulatory issues
Maintain trial documentation including Trial Master Files and Investigator Site Files per GCP standards

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Date posted16 days ago

Last source check1 day ago

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