Live opening · Posted 3 days ago
At a glance
The key details from the original listing.
About the role
Description supplied by the original job listing.
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
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
Employment type
Full-time
Work arrangement
Hybrid
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