Independent Clinical Trial Monitor

5 days ago


Oslo, Oslo County, Norway Optimapharm Full time
Your Role
We are seeking an experienced Clinical Research Associate to join our Clinical Operations team in Norway. As a member of our team, you will play a vital role in supporting our clients and making a tangible difference to project sponsors and benefiting patients worldwide. Your responsibilities will include performing routine site visits, managing assigned sites, and ensuring site compliance with study requirements. You will also identify potential risks, prepare corrective and preventive plans, negotiate study budgets, and administer site payments.

Key Skills
To excel in this position, you should have a strong understanding of ICH GCP Guidelines, regulatory requirements, and clinical research principles. Excellent verbal and written communication skills are necessary, as well as the ability to read, analyze, and interpret common scientific and technical journals. You should be able to work independently, proactively, and effectively in a matrix environment.

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