Clinical Research Associate: Site Monitoring & Compliance

IQVIA in Oslo, Norway, is seeking a skilled professional for site monitoring and management to ensure compliance with study protocols and regulations. The role involves performing site visits, managing study progress, and maintaining communication with sites.

The ideal candidate will have a Bachelor’s degree, at least 2 years of experience in on-site monitoring, and proficiency in regulatory requirements and Microsoft software. Strong problem-solving and communication skills are essential.