➡️ Apply here: Clinical Research Associate (CRA)
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We are looking for an experienced CRA to support international multi-center clinical trials conducted at sites in Tbilisi, Georgia. The role is primarily remote, with regular on-site monitoring visits to assigned sites.
What you’ll do
Perform the full on-site monitoring cycle across assigned Tbilisi sites, including source document verification against primary medical documentation
Manage site communication and maintain compliant trial master file records
Read, review, and interpret source records written in Georgian; facilitate accurate translation of primary medical documentation as part of monitoring activities
Conduct site communication in Georgian to ensure clear and effective interaction with investigators, site staff, and clinical teams
Lead and participate in key trial meetings in English (Investigator Meetings, status calls, vendor calls)
Ensure protocol adherence and compliance with ICH-GCP, sponsor SOPs, and applicable local regulations
Identify and escalate risks and deviations, contribute to CAPA, and support audits and inspections
Collaborate cross-functionally with PM, DM, Safety/PV, Regulatory, and QA teams
What we’re looking for
2+ years of CRA/clinical monitoring experience
Professional proficiency in English (B2 or above)
Professional proficiency in Georgian (C1–C2) — required to independently review primary source medical documentation written in Georgian and to conduct effective on-site communication with investigators and site personnel
Ability to perform regular on-site monitoring visits in Tbilisi as per the monitoring plan
Medical or biomedical education is a strong plus
Nice to have
Experience with audits, inspections, and CAPA processes
Therapeutic area experience in cardiology
Work format Remote, with on-site visits to Tbilisi clinical sites as required by the monitoring plan.