국내 Global CRO 임상 MD.CRA
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MD.CRA
MD.CRA has the responsibility to verify that the rights and well-being of human subjects are protected
and that the reported trial data are accurate, complete, and verifiable from source documents.
Most importantly, the MD-CRA makes sure that the conduct of the trial is in compliance with the currently approved
Clinical Investigation Plan (CIP)/amendment(s), with SOP, with GCP, and with applicable regulatory requirement.
[ 필수사항 ]
- MD.CRA 1년 이상(최소 6개월이상) 또는 CRA 1년 이상(최소 6개월이상)
- 간호사 (우대), 영어가능자 (우대)
MD.CRA has the responsibility to verify that the rights and well-being of human subjects are protected
and that the reported trial data are accurate, complete, and verifiable from source documents.
Most importantly, the MD-CRA makes sure that the conduct of the trial is in compliance with the currently approved
Clinical Investigation Plan (CIP)/amendment(s), with SOP, with GCP, and with applicable regulatory requirement.
[ 필수사항 ]
- MD.CRA 1년 이상(최소 6개월이상) 또는 CRA 1년 이상(최소 6개월이상)
- 간호사 (우대), 영어가능자 (우대)
