Join IQVIA as a Freelance CRA supporting a phase III neurology clinical trial. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.

• Location: Sweden - travel required to Stockholm and Umea
• FTE: around 4h-12 per week
• Start: ASAP
• Duration: 6-12 months

Your 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

Your Profile:

• 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

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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.