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Job Location | Bangalore |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | Sales / BDGeneral / Other Software |
EmploymentType | Full-time |
Review Study protocol and Case Report Forms. Preparation and review of DVS (Data Validation specification). Preparation and review of manual listings for the study. Preparation and review of eCRF Completion guidelines for the study. Performing UAT (User Acceptance Testing) of the edit checks for the study.
Developing eCRF using CDM systems. Programming edit checks and deploys study to production. Performing post production changes and assessment of impact on database. To carry out other responsibilities and as when assigned by the management.
Qualifications
Drug Development and Preclinical Studies In process of validation ,Keyskills :
useracceptancetesting musicmaking datavalidation postproduction useracceptance queryresolution querymanagement drugdevelopment acceptancetesting saereconciliation cdm uat dvs ecrf pharma manual checks testing windows tatementsofworksow