Sr. SAS Programmer
New Jersey All, NJ
*Please only apply if you have SAS Programming experience directly from a pharma, CRO or biotech**
**Experience with Medical Affair Hematology Cancers (i.e. multiple myeloma(MM), chronic leukemia lymphoma (CLL), MDS/AML) studies, and with Registry/EMR data are preferred.
Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells.
Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs.
Perform ad hoc flexible and rapid programming arising from questions generated from planned analyses and results.
Ensure consistency and adherence to standards within their therapeutic area.
Provide programming support for the preparation of integrated reports, submissions and post-submission activities.
Oversee the services provided by CROs.
Contribute to the creation, maintenance, and validation of standards for programming tools, outputs and macros.
Bachelor s degree in life science, statistics, mathematics, computer science, Masters preferred.
8 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions with a Bachelor s degree; or 5 plus years experience with a MS/MA degree.
Experience in Oncology, Hematology Cancer (i.e. CLL) and Medical Affair Projects are preferred.
Demonstrated proficiency in using SAS to produce derived analysis datasets and produce TFLs.
Thorough understanding of clinical data structures, relational database structures, and data exchange with alternate data formats.
Demonstrated expertise in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.
Demonstrated expertise in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.