Clinical Research Associate II / Senior CRA

PSI CRO AG · Kyiv, Ukraine · full-time · Hybrid · September 15, 2026

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Posted September 15, 2026 · Read from PSI CRO
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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.

Qualifications

  • MD, PharmD or MSc
  • 2+ years 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

Hybrid role in Kyiv, 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

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.

Employer
PSI CRO AG
Location
Kyiv, Ukraine · Hybrid
Contract
full-time