Oversees outsourced DM activity of DM CROs and EDC suppliers.
Guides internal clients in establishing case report form requirements and Incorporates simple changes into case report form
Reviews data format specifications for case report forms
Reviews EDC design for clinical trial data management
Reviews prerelease case report form, database and other system related testing
Reviews feedback from user acceptance testing and Complies user feedback review
Reviews the report of Serious Adverse Event reconciliation between the clinical and GMS databases
Reviews clinical data queries generated by DM CRO for data quality assurance of the study
Reviews medical coding conducted by DM CRO

Bachelor’s degrees or above.
3-5 years’ experience in pharmaceutical Medical Affairs is preferred
Interpersonal and communication skills to effectively interact with a broad range of external and internal personnel
Competency to provide guidance to internal clients on development of case report form data requirements
Excellent reading & writing skills in English

- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자