Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

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.

Full-time 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

Qualifications

• 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

Additional Information

• 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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