Incyte Corporation
Biostatistical Programmer
Incyte Corporation, Wilmington, Delaware, us, 19894
Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.Job Summary (Primary function)
The Biostatistical Programmer is responsible for processing clinical data required for the statistical analysis of Phase I - III clinical trials.Essential Functions of the Job (Key responsibilities)
Conduct statistical programming work of clinical data using SAS Software.Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.Generate analysis datasets according to CDISC standard and SAP.Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct adhoc analyses.Validate programs and associated results produced by other programming colleagues.Participate in TLF shell preparation and review, and assist statistician for SAP preparation.Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.Learn, and implement Incyte standard SAS macros for efficient analyses of clinical data supervised by Lead programmers.Qualifications (Minimal acceptable level of education, work experience, and competency)
BA/BS degree in mathematics, statistics, computer science or health related field.2 - 4 years of SAS programming working experience in the pharmaceutical industry.Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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The Biostatistical Programmer is responsible for processing clinical data required for the statistical analysis of Phase I - III clinical trials.Essential Functions of the Job (Key responsibilities)
Conduct statistical programming work of clinical data using SAS Software.Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.Generate analysis datasets according to CDISC standard and SAP.Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct adhoc analyses.Validate programs and associated results produced by other programming colleagues.Participate in TLF shell preparation and review, and assist statistician for SAP preparation.Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.Learn, and implement Incyte standard SAS macros for efficient analyses of clinical data supervised by Lead programmers.Qualifications (Minimal acceptable level of education, work experience, and competency)
BA/BS degree in mathematics, statistics, computer science or health related field.2 - 4 years of SAS programming working experience in the pharmaceutical industry.Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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