• Ensures proper documentation and storage of drug samples for Comparative Dissolution Profile (CDP) testing and Bioequivalence (BE) studies and coordinates receipt and dispatch of drug samples
• Manages and documents the handling and storage of investigational products for Clinical Studies
• Reproduces, organizes and packs the approved study materials and documents according to Good Clinical Practice (GCP) and assist in the preparation of study documents for submission to the Ethics Committee and/or Phil FDA
• Assists in the study-related meetings (GCP training; Site Initiation; Investigator's...