Job Description

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.

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

    • Qualifications

  • MD, PharmD or MSc
  • 2+ years of independent on-site monitoring experience in Ukraine
  • Experience in all types of monitoring visits ...

    • Ready to Apply?

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