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담당업무
Responsibilities : ㆍ Design and review of database structure, validation rules and consistency checks. ㆍ Operation of Clinical Data Management software for data entry of clinical trial results. ㆍAll data cleaning/validation tasks ㆍDevelopment of all key Data Management Documents ㆍLiaison with client companies / monitoring staff as appropriate, ensuring effective study communication with internal and external stake holders ㆍLiaison with external service providers on Data Management projects as appropriate. g. Assist in the development of protocols as requiredㆍPerform comprehensive data management tasks including data review, query management, external data reconciliation
자격요건
ㆍ학력 : 대졸이상
ㆍ경력 : 경력 1년↑
우대사항 ㆍCRS cube builder 경험 1년 이상
ㆍMedDRA certification 소지자 (Medical coding / Manual coding 가능자)
ㆍCRF layout 경험자 또는 SAS 코딩 가능자
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전형절차
ㆍ서류전형 > 폰스크리닝 > 실무진면접 > 레퍼런스체크 > 최종합격
ㆍ면접 일정은 추후 통보됩니다.
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유의사항
ㆍ허위사실이 발견될 경우 채용이 취소될 수 있습니다.
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