Freelance Clinical Research Associate - Sweden
On-siteUmeå, Västerbotten, Sweden
Job Summary
Conduct site evaluations, initiations, monitoring, and close-outs for a phase III neurology clinical trial while ensuring GCP compliance and data integrity. Collaborate with investigators and internal teams to review protocols, study manuals, and eCRFs, and support site staff with training and issue resolution. Track investigational product inventory, attend investigator meetings, and contribute to audit readiness and inspection support. Requires 2+ years of CRA experience, including site monitoring and neurology trials, with strong organizational skills. Available 4-12 hours per week with travel to Stockholm and Umeå. Join IQVIA's team to accelerate innovative medical treatments and improve patient outcomes worldwide.
Required Qualifications
- 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 prioritie
- Travel required to Stockholm and Umea
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