Freelance Clinical Research Associate

Job Summary

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 perform site initiation, routine monitoring, and close-out visits
• 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 Pharma company
• Previous experience in preparation and submissions to Ethics Committees/Regulatory Authorities is preferred
• Driver's license and ability to travel