Specific Requirements Employer will accept a Masters degree in Public Health, Medical Epidemiology or a closelyrelated field of concentration plus 4 years in job offered or Statistical Programmer, SAS Programmingrelated occupation. Employer will accept any suitable combination of education, training and experience.br br br Education or Experience must includebr br 1. SAS programming in the pharmaceutical or biotechnologybr 2. Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listingsbr 3. Design, develop, implement, and maintain software for the monitoring of ongoing studies, reporting, and analysis of clinical trialsbr 4. Provide consistency across protocols within a project on CRFs, database design, analyses files, and tables, listings, and graphsbr 5. Produce data listings, summary tables and graphics for interim and final analyses and publicationsbr 6. Create statistical files for statistical analysisbr 7. Integrate data across studies within a projectbr 8. Test, document, review and validate all programs according to department guidelinesbr 9. Provide consulting and systems support for applications softwarebr 10. Develop new applications software and identify key feature setbr 11. Regression analysis, modeling dependent and independent variables, including analysis and documentation for data element correlation and causal relationships linkage and analysisbr 12. SAS CertificationsBase; Clinical Trials Programmer; Advanced Programmingbr 13. CDISC Standards and FDA Submissions

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