Clinical Research Associate / Senior CRA

PSI CRO·Kyiv, Kyiv city, Ukraine

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About the role

Remote Clinical Research Associate / Senior CRA role based in Ukraine. The position involves preparing, conducting and reporting monitoring visits across Phase II and/or III studies, ensuring ICH-GCP and regulatory compliance, managing site documentation and risks, supporting submissions and audits, and training site staff. MD, PharmD or MSc, at least one year of independent on-site monitoring experience in Ukraine, English and Ukrainian proficiency, MS Office skills, and travel ability are required.

Key requirements

• MD, PharmD or MSc
• At least 1 year of relevant experience
• Required skills: independent on-site monitoring experience in Ukraine, monitoring visits including site selection, initiation, routine monitoring and close-out, Phase II and/or III clinical trial experience, ICH-GCP compliance, regulatory requirements compliance, source data verification, data query follow-up, investigational product accountability, trial supplies and essential study documentation management, Investigator Site File maintenance, Trial Master File reconciliation, study-specific training delivery, regulatory submissions support, audit preparation, audit finding resolution, MS Office proficiency, English, Ukrainian, planning, multitasking, communication, collaboration, problem-solving, ability to travel
• Required languages: English, Ukrainian

Opportunity details

• Workplace: Remote
• Posted: Oct 16, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Clinical Research Associate / Senior CRA

Location: Kyiv, Kyiv city, Ukraine

Employment type: Full-time

Workplace type: Remote

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. You will be collaborating with experienced clinical research professionals who are committed to quality, teamwork, and advancing clinical research.

Remote role in Ukraine

Your responsibilities will include:

Preparing, conducting, and reporting on all types of monitoring visits, including site selection, initiation, routine monitoring, and close-out visits
Ensuring compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
Building and maintaining strong relationships with investigators and site staff
Monitoring patient recruitment, study timelines, and site performance
Performing source data verification, following up on data queries, and managing site-level risks
Overseeing investigational product accountability, trial supplies, and essential study documentation
Maintaining Investigator Site Files (ISF) and supporting Trial Master File (TMF) reconciliation
Delivering study-specific training to investigators and site staff
Supporting regulatory submissions, audit preparation, and resolution of audit findings

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.