Job Description
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
