Clinical Research Associate at PSI CRO

Tbilisi, , Georgia -

Full Time

Start Date

Immediate

Expiry Date

31 Dec, 25

Salary

0.0

Posted On

02 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Monitoring, Study Startup, CRF Review, Source Document Verification, Query Resolution, Site Communication, Project Management, Feasibility Research, Regulatory Support, MS Office Proficiency, Communication Skills, Collaboration Skills, Problem-Solving Skills, Multitasking, Teamwork

Industry

Pharmaceutical Manufacturing

Description

Company 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. 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

Responsibilities

As a Clinical Research Associate, you will conduct and report onsite monitoring visits and be involved in study startup activities. You will also manage site communication and support internal project teams regarding study progress.