高级临床监查员（SCRA）外派

1. In charge of the selection of potential/qualifie******** according toprotocol.
2. In charge of EC submission
3. Discuss thoroughly with investigators an******** staff in theimplementation of the protocol/agreements
4. Perform monitoring visit for clinical trials in compliance with thecurrently approve********/amendment(s), with GCP, an******** theapplicable regulatory requirement(s)
5. Ensure that all AEs an******** are appropriately reporte******** thetime periods.
6. Provide support to PM in project management
7. Assist in protocol review an******** design/revie********

Qualification********
1. A bachelor degree in Medicine or Pharmacy. Advance******** such as MSis desirable.
2. More than 2 years experience of clinical monitoring .pharmaceuticalcompany.
3. Goo******** skill an******** attitude.
4. Fluency in written an******** English.