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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Medical / Healthcare |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
*Provides SAS / Statistical programming support & advice team primarily using SAS software.Reports to local India Manager/Principal Programmer.Works across international and functional boundaries as needed within a project team environment.Works closely with Statistics and Data Management team members.Review protocols, CRFs, annotated CRFs, test databases and Statistical Analysis PlansDevelop, test and produce CDISC SDTM/ADAM datasets, derived datasets, tables, listings and graphs for clinical study reports.Validate team primarily using SAS software, derived datasets, tables, listings and graphs for clinical study reports.Importing and exporting data filesExtraction of data from database (e.g. Clintrial)Assist with Quality Control ActivitiesAssist with development of departmental guidelines in line with the standardization of programs and systems for the generation of CSR componentsGenerate and maintain study documentationAttend and participate in project team meetings, *Bachelor s degree in Statistics, Computer Science, Mathematics or related discipline.Good SAS programming skills with 3 years experience in the pharmaceutical industry or a clinical research organization.Skills should include Base SAS, SAS Macro and SAS ODS.Good understanding of CDSC SDTM/ADAM standards.Basic understanding of Software Development Lifecycle.Good verbal and written communication skills.Ability to work independently on multiple projects, plan, organize and prioritize activities.
Keyskills :
sassas programmingsdtmdata managementreportingstatistical analysis plansbase sasquality controlcomputer scienceclinical researchsoftware developmentstatistical analysis