Clinical Research Coordinator
Unilab, Inc. Mandaluyong
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 Meeting) , procurement of study equipment and supplies, and proper filing of all study-related documents
- Documents clinical study team meetings and discussions with divisions
- Tracks Clinical Research for on-going projects
- Graduate of a Bachelor's Degree
- Preferably a degree holder of Health Sciences-related courses, including but not limited to Nursing, Pharmacy, Medical Technology, Biology, or related disciplines
- Must have at least 1 to 2 years of relevant professional work experience, preferably within healthcare, pharmaceutical, clinical, or similar industries
- Detail-oriented, demonstrating strong accuracy and thoroughness in performing tasks and delivering outputs
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