Mô tả công việc
CRA for BE study/New drugs/Medical devices
1.Clinical research study setup/study procedure setup/site staff training
2.Site monitoring visits/source data verification/deviation reporting in compliance with GCP
3.Trial documents maintenance/regular site visits and maintenance/study materials supply/interim reports
4.regular report to sponsor/communication between sponsor and site.
5.site close-out/trial materials retrieval
6.audits/regulatory inspection participation upon request
Số lượng tuyển dụng
1~1人
Trình độ học vấn
大學(學院)以上
Yêu cầu ngành học
醫藥衛生學科類、醫學系相關、護理助產相關
Giờ làm việc
08:30~17:30
Chế độ nghỉ
週休二日
Loại công việc
Other Project Managers
Biotechnology Research and Development Staff
Pharmaceutical Research and Development Staff