IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research
- 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
