About this role
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. Role is combined with office and home-based in Ukraine. All CV's needs to be submitted in English language. Responsibilities: 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, assit in agreements University degree in Life Science field Fluent English and local language Independent monitoring experience as a CRA In depth therapeutic and protocol knowledge Deep knowledge in clinical research regulatory requirements (GCP and ICH) Excellent skills in MS Office, EDC and other clinical trial related systems and platforms Attention to detail and time-management skills Professional growth and career opportunities International team and environment Bonus based on annual performance Personal accident and business trip insurance Additional health insurance Remote/home based Complimentary health and wellness benefits, such as influenza vaccines Rewarding referral policy Workplace establishment allowance (fully remote) Team building, global meetings, B active events