--- title: Clinical Trial Coordinator at GM Pharma description: GM Pharmaceuticals is looking for a Clinical Coordinator to join its Research & Development team and support international clinical and bioequivalence studies. Location: Tbilisi, Georgia, Kvemo Ponich --- # Clinical Trial Coordinator **Company:** GM Pharma **Location:** Georgia **Posted:** 2026-10-15 **Apply by:** 2026-11-29 [Apply / View original posting](https://www.linkedin.com/jobs/view/4477085319) ## Job description GM Pharmaceuticals is looking for a Clinical Coordinator to join its Research & Development team and support international clinical and bioequivalence studies. Location: Tbilisi, Georgia, Kvemo Ponichala — fully on-site Department: Research & Development (R&D) Key Responsibilities Coordinate clinical and bioequivalence studies with international Contract Research Organizations (CROs). Support study planning, execution, monitoring, and timely completion. Review study protocols, documentation, monitoring reports, and clinical study reports. Track milestones, deviations, corrective actions, and deliverables. Collaborate with investigators, clinical monitors, CROs, and internal teams. Participate in international monitoring visits, CRO assessments, and study-related visits. Maintain accurate study records and provide progress updates to R&D management. Qualifications and Experience Bachelor’s or Master’s degree in Pharmacy, preferably with a specialization in Pharmacology, Medicine, or Clinical Sciences. Experience in clinical studies, clinical monitoring, bioequivalence studies, or CRO coordination is preferred. Knowledge of Good Clinical Practice (GCP), clinical documentation, and regulatory requirements is an advantage. Proficiency in Microsoft Excel and PowerPoint, with the ability to prepare scientific reports and presentations. Fluent written and spoken English; Russian language skills are an advantage. Motivated graduates with strong scientific aptitude and a willingness to learn are welcome to apply. Key Competencies Strong communication, interpersonal, and collaboration skills. Analytical thinking and a scientific approach to problem-solving. Strong organizational skills, responsibility, and attention to deadlines. A proactive, adaptable approach and openness to feedback and learning. Working Conditions and Travel Fully office-based role in Tbilisi, Georgia. Willingness to undertake occasional international travel for clinical monitoring, CRO assessments, and project activities, including visits to CIS countries, Europe, Jordan, and India. Flexibility to coordinate with international partners across different time zones How to Apply Please send your CV in English --- 🔔 [Monitor similar jobs on Gurify](https://gurify.com/?utm_source=techgeo&utm_medium=jobboard&utm_campaign=monitor_similar&role=Clinical+Trial+Coordinator) — get alerted when matching roles are posted in Georgia. ```json {"@context":"https://schema.org/","@type":"JobPosting","title":"Clinical Trial Coordinator","description":"

GM Pharmaceuticals is looking for a Clinical Coordinator to join its Research & Development team and support international clinical and bioequivalence studies. Location: Tbilisi, Georgia, Kvemo Ponichala — fully on-site Department: Research & Development (R&D) Key Responsibilities Coordinate clinical and bioequivalence studies with international Contract Research Organizations (CROs). Support study planning, execution, monitoring, and timely completion. Review study protocols, documentation, monitoring reports, and clinical study reports. Track milestones, deviations, corrective actions, and deliverables. Collaborate with investigators, clinical monitors, CROs, and internal teams. Participate in international monitoring visits, CRO assessments, and study-related visits. Maintain accurate study records and provide progress updates to R&D management. Qualifications and Experience Bachelor’s or Master’s degree in Pharmacy, preferably with a specialization in Pharmacology, Medicine, or Clinical Sciences. Experience in clinical studies, clinical monitoring, bioequivalence studies, or CRO coordination is preferred. Knowledge of Good Clinical Practice (GCP), clinical documentation, and regulatory requirements is an advantage. Proficiency in Microsoft Excel and PowerPoint, with the ability to prepare scientific reports and presentations. Fluent written and spoken English; Russian language skills are an advantage. Motivated graduates with strong scientific aptitude and a willingness to learn are welcome to apply. Key Competencies Strong communication, interpersonal, and collaboration skills. Analytical thinking and a scientific approach to problem-solving. Strong organizational skills, responsibility, and attention to deadlines. A proactive, adaptable approach and openness to feedback and learning. Working Conditions and Travel Fully office-based role in Tbilisi, Georgia. Willingness to undertake occasional international travel for clinical monitoring, CRO assessments, and project activities, including visits to CIS countries, Europe, Jordan, and India. Flexibility to coordinate with international partners across different time zones How to Apply Please send your CV in English

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