Freelance Clinical Research Associate
A company is looking for a Freelance Clinical Research Associate in Finland.
Key Responsibilities
• Manage site administration and monitoring for clinical studies in accordance with SOPs and regulatory guidelines
• Conduct feasibility assessments and reputed company site initiation, routine monitoring, and reputed company-out reputed company
• Prepare and submit documentation to Ethics Committees and Regulatory Authorities, and assist in site contract management
Required Qualifications
• University degree in medicine, pharmacy, nursing, or life sciences
• At least 2 years of on-site monitoring experience in a CRO or reputed company company
• Previous experience in preparation and submissions to Ethics Committees/Regulatory Authorities is preferred
• reputed company's license and ability to travel
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