UST Center for Drug Research Evaluation and Studies, Inc. is an internationally recognized center of scientific excellence for drug research, evaluation and studies that provide credible, safe and quality services to meet Bioavailability/Bioequivalence studies and clinical study requirements of our sponsors. An ISO 17025:2005 and ISO 15189:2007 accredited and complies with Good Clinical Practice (GCP) and Good Laboratory Practice (GLP).
Central Luzon, National Capital Reg, Northern Mindanao
Responsibilities:
1. Serves as the main line of communication between the sponsor and trial sites
2. Oversee Clinical Research Associates to monitor trial sites
3. Supervises the total project
4. Prepares write-up of the project plan
5. Leads the project training
6. Set-up the investigator meeting
7. Responsible for over-all project deliverables
8. Prepare resource allocation
9. Responsible for risk management
10. Mentors and evaluates performance of Clinical Research Associates
Requirements:
- A degree in medical science or medical science-related courses (preferably licensed)
- Proficient in oral or written english
- With management and communication skills
- At least with 5 years experience in related fields
- Computer literate
- Can work individually or as a team member
- Must be willing to work in Alabang
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