Research Analyst

• Join our dynamic team at Biomapas as a Clinical Research Associate (CRA) in Ukraine.
• Your role will be crucial in overseeing clinical trials and ensuring that they are conducted in compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Study site monitoring and management (site selection, initiation, monitoring and close-out visits)
• Perform feasibilities and support start-up phase
• Create and maintain required study documentation (site management, monitoring, etc.)
• Ensure that clinical trials are conducted according to requirements (protocol, ICH-GCP, etc.)
• Administer protocol and related study training to assigned sites
• Perform regulatory document review
• Prepare clinical trial documents and store, archive correspondence
• Negotiate study budgets with potential investigators/sites, assist in agreements

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Clinical Research Associate