Clinical Research Associate (CRA) Ukraine
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Before you apply
LocationKyiv, Kyiv city, Ukraine
Work modehybrid
Typefull-time
SenioritySenior
DepartmentClinical Operations (CO)
Company size51–200 people
First seenSep 11, 2026 · 1mo ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
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
Skills
MS Office
EDC
Benefits
Professional growth and career opportunities
International team and environment
Performance bonus
Business trip insurance
Health insurance
Hybrid work
Wellness benefits
Referral bonus
Remote allowance
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.
Hiring process
CV needs to be submitted in English language
Responsibilities:
•
Study site monitoring and management (site selection, initiation, monitoring and close-out visits)
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Perform feasibilities and support start-up phase
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Create and maintain required study documentation (site management, monitoring, etc.)
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Ensure that clinical trials are conducted according to requirements (protocol, ICH-GCP, etc.)
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Administer protocol and related study training to assigned sites
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Perform regulatory document review and submission to regulatory authorities
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Prepare clinical trial documents and store, archive correspondence
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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.
•
Rewarding referral policy
•
Workplace establishment allowance (fully remote)
•
Team building,AND global meetings.