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Clinical Research Associate II / Senior CRA

psicro

Tbilisi, Tbilisi, Georgia permanent

Posted: April 29, 2026

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Quick Summary

The Clinical Research Associate II/Senior CRA is responsible for conducting high-quality clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to deliver timely and successful studies.

Job Description

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

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.

Office-based in Tbilisi, Georgia

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 
• Experience working in a clinical site as a study coordinator or sub-investigator is a plus
• Independent on-site monitoring experience in Georgia 
• Full working proficiency in English and Georgian
• 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

 

• PSI is a stable, privately-owned company, organically growing since 1995
• We have an excellent reputation in the industry, having won the CRO Leadership awards several years in a row
• Team collaboration is high on our agenda. Our aim is for employees to feel valued and heard in friendly and supportive teams
• We offer extensive training programs, profound therapeutic area trainings, monitors training program, mentorship programs, interactive soft-skills trainings and more
• PSI CRAs have an opportunity to work with different Sponsors on a variety of therapeutic areas
• We have a large portfolio of projects, mostly phase II and III
• Each monitor will work on a limited number of protocols, thus ensuring they can give the best support to the sites
• We have comfortable office facilities with easy commute, corporate benefits, refreshers and team building events

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