• Responsibilities:

  * Design and review of database structure, validation rules and consistency checks.
  * Operation of Clinical Data Management software for data entry of clinical trial results.
  * All data cleaning/validation tasks 
  * Development of all key Data Management Documents 
  * Liaison with client companies / monitoring staff as appropriate, ensuring effective study communication with internal and external stake holders 
  * Perform comprehensive data management tasks including data review, query management, external data reconciliation

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• 2명
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• 학력 : 대학교(4년) 졸업
• 성별 : 성별무관
• 나이 : 연령무관

Minimum Qualifications & Experience: 

•  * At least 1~2 years of DM experience in the pharmaceutical or CRO industry. 
•  * Medical data review
•  * Medical coding 
•  * CMC(Certified MedDRA Coder) / 약사 우대.