კლინიკური კვლევების კოორდინატორი

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.