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Job Overview
• Supports and manages relationships with pharmacies in global clinical trials up to Phase III with a special focus on clinical trials conducted in the region
• Contact for IMP-related and Clinical Trial Supply Management (CTSM) -related questions for CROs/ Sites / pharmacies
• Contributes to training CROs and site personnel on IMP handling
• Liaises with GCP QA and supports CTSM GCP related activities
• Supports on appropriate CTSM GCP risk communication and ensures CTSM GCP requirements are met
• Manages complaints, deviations, changes, and other quality incidents for GCP topics
• Travel requirement: 15%

Qualifications
• Relevant professional experience (usually +3 years) in Clinical Supply or Clinical Research in Pharmaceutical/Biotech industry or CRO setting or any equivalent e.g., Pharmacy Services
• Relevant completed university education in Pharmacy, experience as a Clinical Pharmacist or in an equivalent role
• Deep understanding of country-specific requirement and standards for Clinical Trials conducted in the region
• Deep Knowledge about Pharmacy Manuals / Pharmacy Questionnaires
• Deep Knowledge about GCP principles (e.g., Ethical Principles, Adequate Drug Information, etc.)
• Business-professional English and local language skills
• Self-motivated with strong problem-solving and learning skills
• Ability to create independent analyses and develop new solutions
• Excellent organizational and communicative skills
• Enjoys working in a team
• Openness to explore on new topics for setting up the trend