Global Channel Management, Inc.
SAS Programmer III
Global Channel Management, Inc., South San Francisco, California, us, 94083
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day-to-day function. Organizations need to reduce training and labor costs while still requiring the best talent for the job.Qualifications
Bachelors or Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific subjects.8+ years clinical research and development statistical programming experience using SAS.Performs all SAS programming required for clinical trial analysis and reporting.Ensures that activities and processes performed are conducted according to sponsor requirements.Works closely with the Biostatistics and Data Management departments on various clinical projects.Leads programming efforts for large complex studies.Requires time management skills and strong SAS programming expertise.Reviews case report form (CRF) design.Designs and/or reviews database structure.Writes, tests, and validates SAS programs to produce analysis datasets, TLGs, and presentation output for reports submitted to regulatory agencies, publications, and other communications.Writes CDISC standard dataset specifications and follows specifications to create SDTM and ADaM datasets.Understands and executes department-, product-, and study-level macros and utilities.Writes, tests, and validates product- and study-level macros and utilities.Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR).Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses.Years of Experience: 5-7.Strong SAS Programming skills.Extensive hands-on experience in CDISC standards and datasets (SDTM, ADaM).Experience in FDA/EMEA trial submissions.Drug Development (pre-, early, late, and/or observational) in related industries or academic research.
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Bachelors or Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific subjects.8+ years clinical research and development statistical programming experience using SAS.Performs all SAS programming required for clinical trial analysis and reporting.Ensures that activities and processes performed are conducted according to sponsor requirements.Works closely with the Biostatistics and Data Management departments on various clinical projects.Leads programming efforts for large complex studies.Requires time management skills and strong SAS programming expertise.Reviews case report form (CRF) design.Designs and/or reviews database structure.Writes, tests, and validates SAS programs to produce analysis datasets, TLGs, and presentation output for reports submitted to regulatory agencies, publications, and other communications.Writes CDISC standard dataset specifications and follows specifications to create SDTM and ADaM datasets.Understands and executes department-, product-, and study-level macros and utilities.Writes, tests, and validates product- and study-level macros and utilities.Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR).Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses.Years of Experience: 5-7.Strong SAS Programming skills.Extensive hands-on experience in CDISC standards and datasets (SDTM, ADaM).Experience in FDA/EMEA trial submissions.Drug Development (pre-, early, late, and/or observational) in related industries or academic research.
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