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Title:Sr. SAS Programmer
Location:MA - Lexington

The programmer will develop and maintain general-purpose and ad hoc SAS programs for the analysis and reporting of clinical and/or post marketing data, perform QC task to ensure accuracy, and participate in functional process and technology initiatives.


·        Provide general SAS programming support to Clinical Research and Development.

·        Work closely with statisticians to generate analysis data sets and create tables, listings and graphs for interim analyses, preliminary reports and Clinical Study Reports for in-house use, publications, and/or regulatory submissions.

·         Perform quality control checks on program code and outputs produced by other team members.

·         Conduct data edit checks to ensure the quality of source data.

·        Enhance existing utility programs and develop new utility macros to standardize data processing and output procedure.

·        Review and provide input on programming related documentation including plans and specifications.

·        Manage programming timelines, schedules, and activities on specific programming tasks.

·        Report to Associate Director of Statistical Programming.


·       Bachelor's degree in life science, statistics, mathematics, computer science, or related field required; Master's degree preferred.

·        5+ years of SAS programming experience in biotech or pharmaceutical industry.

·         Experience in SAS programming language, macros, and procedures.

·         Working knowledge of ISS/ISE, CDISC standards (SDTM, ADaM).

·         Detail oriented and strong organizational and communication skills.

·         Ability to work in a team environment.

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