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Position: Senior Statistical Programmer
Institution: Novavax, Inc.
Location: Gaithersburg, Maryland, United States
Duties: Programmatically support all statistical programming and related activities in Phase I - Phase III clinical trials for seasonal flu and COVID19 vaccines; Writing SAS programs from instructions provided by Biostatisticians to create CDISC datasets as well as tables, figures, and listings of clinical trials for vaccine studies; Create and validate SAS datasets to map data exported from database (such as CSV files) according to specifications; Collaborate with Biostatistics and Clinical Operations on edit checks or data review
Requirements: BS degree in Statistics, Computer Science, or related field; Eight to eleven years SAS programming experiences (Base SAS, SAS/STAT, and SAS macro language) on phase I, II, or III clinical trial data, in creating/validating SAS datasets and TFLs (per SAP/table shell/specs) for CSR in pharmaceutical, biotech, or CRO companies; Programming experience in producing outputs for periodical safety report (such as SRT, DSMB, DSUR, or ClinicalTrials.gov), or outputs to support publications
   
Text: Senior Statistical Programmer Programmatically support all statistical programming and related activities in Phase I - Phase III clinical trials for seasonal flu and COVID19 vaccines; Writing SAS programs from instructions provided by Biostatisticians to create CDISC datasets as well as tables, figures, and listings of clinical trials for vaccine studies; Create and validate SAS datasets to map data exported from database (such as CSV files) according to specifications; Collaborate with Biostatistics and Clinical Operations on edit checks or data review BS degree in Statistics, Computer Science, or related field; Eight to eleven years SAS programming experiences (Base SAS, SAS/STAT, and SAS macro language) on phase I, II, or III clinical trial data, in creating/validating SAS datasets and TFLs (per SAP/table shell/specs) for CSR in pharmaceutical, biotech, or CRO companies; Programming experience in producing outputs for periodical safety report (such as SRT, DSMB, DSUR, or ClinicalTrials.gov), or outputs to support publications
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