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
- 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
