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
Apply via :
jobs.iqvia.com