Full-time
Clinical Research Associate I/II — Site Monitoring
Posted by IQVIA LLC • Espoo, Uusimaa, Finland
About the Role
A global clinical research firm is seeking a Clinical Research Associate to perform monitoring and site management duties in Espoo, Finland. The ideal candidate will have at least 1 year of monitoring experience and knowledge of Good Clinical Practice (GCP). Responsibilities include conducting site visits, managing study progress, and ensuring compliance with regulations. This is a full-time position offering significant opportunities for professional growth and contribution to improving patient outcomes.
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