Global Clinical Operations Expert

5 days ago


Oslo, Oslo County, Norway Optimapharm Full time
Responsibilities and Requirements
This role involves working independently as a Clinical Research Associate on our Clinical Operations team in Norway. Your primary responsibilities will include performing routine site visits, managing assigned sites, and ensuring site compliance with study requirements. You will identify potential risks, prepare corrective and preventive plans, negotiate study budgets, and administer site payments. To succeed in this role, you should possess a university degree in medical or life sciences, preferably with nursing education or other relevant healthcare college degree. At least 3-4 years of independent clinical trial monitoring experience is required, along with a high level of knowledge of ICH GCP Guidelines and regulatory requirements.

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