Clinical Research Associate (CRA) Ukraine

Join our global team as a (Senior) Clinical Research Associate (CRA) in Ukraine.

Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of studies and clinical trials at investigational sites.

_Role is combined with office and home-based in Kyiv, Ukraine._

_CV 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 and submission to regulatory authorities
• Prepare clinical trial documents and store, archive correspondence
• Negotiate study budgets with potential investigators/sites, assist in agreements
• Provide monitoring visits and site management

Requirements

• 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

Benefits

• Professional growth and career opportunities
• International team and environment
• Bonus based on annual performance
• Personal accident and business trip insurance
• Additional health insurance
• Hybrid mode of work
• Complimentary health and wellness benefits, such as influenza vaccines
• Rewarding referral policy
• Workplace establishment allowance (fully remote)
• Team building, global meetings, B active events