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 UmeaFTE: around 4h-12 per weekStart: ASAPDuration: 6-12 months

Your Role

Conduct site evaluations, initiations, monitoring & close-outsEnsure GCP compliance and data integrityCollaborate with investigators and internal teamsReview protocols, study manuals, and eCRFsSupport site staff with training and issue resolutionTrack investigational product inventory and documentationAttend investigator meetings and study-related eventsContribute to audit readiness and inspection support

Your Profile:

2+ years CRA including site monitoring experienceExperience in Neurology trialsStrong knowledge of clinical trial processes & GCPExcellent communication & organizational skillsAbility to work independently and manage prioritiesFluent in English and Portuguese

If you're ready to make an impact in clinical research, apply today!

#LI-HCPN

#LI-CES

#LI-DNP

#LI-NS1

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.