SAS Programmer III
Target Pay Rate: 75-90/hr **salary will be commensurate with experience
Job Description: • Review and ensure accurate and high-quality statistical programming deliverables from CRO • Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and guidance documents. • Create and maintain specifications as per SDTM/ADaM standard and study SAP. • Define and create ad-hoc reports and listings for clinical teams. • Develop, implement and maintain SAS programming standards. • Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as necessary. • Verifies completeness of relevant study deliverables prior to release from the group • Maintains all required study documentation. • Consults and provides input into system validation efforts including tool maintenance activities. • Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy. • Work in tandem with Biostatistics and Data Management member on various clinical projects. • Review CRF annotations and data specifications. • Perform quality control on final reports. • Develop SAS coding and table templates for preparing, processing and analyzing clinical data. • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues. Skills:- Develop SAS coding for generating SDTM, ADaM datasets and TLFs to support clinical study analysis.
- Perform clinical study report and/or exploratory analysis for oncology clinical study.
- Perform validation of ADaM datasets and TLFs per SAP.
- Effectively review and comment on vendor programming deliverables and help resolve technical difficulties.
- Proficient computer skills across multiple applications and OS environments.
- Oncology experience is highly preferred.
- BS or above in computer science/statistics with at least 5 years of SAS experience in major pharma or CRO.
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