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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- 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
Requirements
What you’ll need- 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
Comp & perks- 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
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial managementregulatory document reviewstudy documentationfeasibility assessmentprotocol knowledgeGood Clinical Practice (GCP)International Council for Harmonisation (ICH)site monitoringbudget negotiationclinical research
Soft Skills
attention to detailtime managementcommunicationindependent monitoringtraining administration
