• 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

• 
  

• 2명
• 
  

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

Minimum Qualifications & Experience: 

•  * At least 5 years of DM experience in the pharmaceutical or CRO industry. 
•  * Medidata 또는 CRScube EDC 개발 가능자 & SAS 코딩 가능자 또는 CRF Layout 개발 가능, MedDRA certification 소지자/경험자