Statistical Programmer Job at Katalyst Healthcares & Life Sciences
Responsibilities:
- Perform clinical trial database quality/integrity checks by generating SAS data listings, summary tables, and graphs for data reviewing and cleaning.
- Develop SAS programs and generate complete, accurate and validated statistical TLGs in well-defined formats.
- Program SDTM and ADaM datasets according to the dataset specifications.
- Create SDTM annotated patient Case Report Forms.
- Develop SDTM dataset specifications under the supervision of a Sr Statistical Programmer or a Biostatistician.
- Perform data conversion between datasets with two different formats according to conversion requirements/specifications, e.g., converting from Excel data records to SAS datasets, non-CDISC compliant datasets to CDISC compliant datasets.
- Manage electronic data transfers from trial sponsors or other external clinical trial data vendors, such as central laboratories or other specialty laboratories.
- Document data and programming information in accordance with Corporate Governing Documents (Policies, SOPs, or Work Instructions).
- Archive clinical trial data (raw data, SDTM, and ADaM datasets) and programming documentation in accordance with Corporate Governing Documents and/or clinical trial sponsor's specific requirements.
Requirements:
- A Master's degree in Statistics, Biostatistics, Bioinformatics, Computer Sciences, and Mathematics, or other relevant fields required.
- At least one year of experience using SAS.
- SAS certification for Base, Advanced, and Clinical Trials Programmers highly preferred.
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