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Job Description
- Responsible for implementation of GCP.
- Supervise the implementation of the ethics committee and review the meeting result.
- Manage recruiting, selection, and screening of study subjects.
- Supervising the withdrawal, separation, packaging, and final destruction of plasma samples.
- Responsible for communication with contracted medical lab.
- Management of study phases.
Job Requirements
- Bachelor's degree in pharmaceutical science or science
- +5 years of experience in the same field.
- Knowledge of the clinical research process, including GCP
- Males only
