该职位来源于猎聘 职责描述:
- Act as the main line of communication between the sponsor and the investigator
- Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout
- Responsible for the safety and proper conduct throughout the trial
- Verifying that the investigator follows the approved protocol and all GCP procedures
- Verifying that source data/documents and other trial records are accurate, complete, and maintained
- Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs
- Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience 任职要求:
- Strong knowledge in ICH-GCP
- Ability to review and evaluate clinical data
- Computer literacy desirable
- Good oral and written communication skills
- Due to the nature of this position it may be required for the employee to travel
- Bachelor degree, or local equivalent, in medicine, science or related discipline