Clinical Research Associate / Senior CRA
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About the role
PSI seeks a Clinical Research Associate / Senior CRA for a hybrid, described as remote, role in Ukraine. The position involves onsite monitoring visits, study startup, CRF review, source document verification, query resolution, site management, feasibility research, regulatory submission support, and coordination with project teams and vendors. Applicants need an MD, PharmD or MSc, at least one year of independent onsite monitoring experience in Ukraine, Phase II/III monitoring experience, English and Ukrainian proficiency, MS Office skills, and travel availability.
Key requirements
- • MD, PharmD or MSc
- • At least 1 year of relevant experience
- • Required skills: Independent on-site monitoring experience in Ukraine, All types of monitoring visits in Phase II and/or III trials, Study startup, CRF review, Source document verification, Query resolution, Site communication and management, Vendor and in-house support coordination, Study progress communication, Feasibility research, Regulatory submission document support, MS Office proficiency, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
- • Required languages: English, Ukrainian
Opportunity details
- • Workplace: Hybrid
- • Posted: Oct 14, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Clinical Research Associate / Senior CRA
Location: Kyiv, Kyiv city, Ukraine
Employment type: Full-time
Workplace type: Hybrid
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
As a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
Remote role in Ukraine
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Qualifications
- MD, PharmD or MSc
- 1+ year of independent on-site monitoring experience in Ukraine
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology/Ulcerative Colitis/Antibiotics trials is a plus
- Full working proficiency in English and Ukrainian
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Oct 16, 2026