Katalyst CRO
Overview
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Senior Statistical Programmer
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Katalyst CRO Responsibilities Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures, and tables. Independently, develop SAS application code. Independently, perform validation of SAS programs and deliverables. Independently, perform migrations and verifications. Independently, perform SDTM and ADaM mapping. Generate SDTM and ADaM deliverables. Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and Client. Generate data files and/or output for safety updates, publications and meeting presentations. Interface with a cross-function of client and Datacentric team members. Act as an Expert in one or more areas that may include Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries or other areas.
Requirements
Background in statistics and statistical analysis is desirable. 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming. Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming. Working knowledge of CDISC, SDTM and ADaM. Expert knowledge of SAS-based statistical programming. Proficiency in SAS programming on multiple platforms and operating systems, e.g., Windows, UNIX, etc. is desirable.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Information Technology
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Join to apply for the
Senior Statistical Programmer
role at
Katalyst CRO Responsibilities Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures, and tables. Independently, develop SAS application code. Independently, perform validation of SAS programs and deliverables. Independently, perform migrations and verifications. Independently, perform SDTM and ADaM mapping. Generate SDTM and ADaM deliverables. Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and Client. Generate data files and/or output for safety updates, publications and meeting presentations. Interface with a cross-function of client and Datacentric team members. Act as an Expert in one or more areas that may include Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries or other areas.
Requirements
Background in statistics and statistical analysis is desirable. 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming. Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming. Working knowledge of CDISC, SDTM and ADaM. Expert knowledge of SAS-based statistical programming. Proficiency in SAS programming on multiple platforms and operating systems, e.g., Windows, UNIX, etc. is desirable.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Information Technology
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr