Freelance Clinical Research Associate
IQVIA
part-time
Posted on:
Location Type: Office
Location: Stockholm • Sweden
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Tech Stack
About the role
- Conduct 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
Requirements
- 2+ years CRA including site monitoring experience
- Experience in Neurology trials
- Strong knowledge of clinical trial processes & GCP
- Excellent communication & organizational skills
- Ability to work independently and manage priorities
- Fluent in English and Portuguese
Benefits
- Travel required to Stockholm and Umea
- Part time hours (around 4h-12 per week)
- Opportunity to work on phase III neurology clinical trial
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
site evaluationsmonitoringGCP compliancedata integrityprotocol reviewstudy manualseCRFsinvestigational product inventoryaudit readinessinspection support
Soft Skills
communicationorganizational skillsindependencepriority management