Clinical Research Associate / Senior CRA

PSI CRO·Kyiv, Kyiv city, Ukraine

Share role

Add a personal message

Email WhatsApp ↗

The recipient sees their own assessment. Your profile and score are not shared.

Role link

About the role

Remote Clinical Research Associate / Senior CRA role in Ukraine involving monitoring visits across Phase II and/or III studies, protocol and ICH-GCP compliance, site and patient recruitment oversight, source data verification, investigational product accountability, study documentation, training, regulatory submissions, and audit support. Requires 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.

Key requirements

• MD, PharmD or MSc
• At least 1 year of relevant experience
• Required skills: Independent on-site monitoring experience in Ukraine, Experience with site selection, initiation, routine monitoring, and close-out visits, Experience in Phase II and/or III trials, ICH-GCP compliance, Regulatory compliance, Source data verification, Data query follow-up, Site-level risk management, Investigational product accountability, Trial supplies management, Investigator Site File maintenance, Trial Master File reconciliation, Study-specific training delivery, Regulatory submissions, Audit preparation, MS Office applications, Ability to travel, English and Ukrainian proficiency, Planning, Multitasking, Communication, Collaboration, Problem-solving
• Required languages: English, Ukrainian

Opportunity details

• Workplace: Remote
• Posted: Nov 10, 2026
• Original advert language: English

Full vacancy

HealthRoleIQ regularly verifies this opportunity against the employer’s posting and highlights the details relevant to your match.

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.