Clinical SAS Programmer

Our client is seeking a Clinical SAS Programmer to support statistical programming activities across active and upcoming clinical trials. You'll play a central role in turning raw clinical data into submission-ready datasets and outputs. Key ResponsibilitiesDevelop, validate, and maintain SDTM and ADaM datasets in accordance with CDISC standardsProgram tables, listings, and figures (TLFs) for clinical study reports, DSMB packages, and regulatory submissionsWrite and QC SAS macros and programs for data derivations and edit checksCollaborate with biostatisticians to implement statistical analysis plans (SAPs)Support define.xml and reviewer's guide development for regulatory submissionsPerform independent programming for QC/validation of key outputsContribute to programming specifications and standard macro libraries as the client's pipeline scalesQualificationsBachelor's or advanced degree in statistics, computer science, life sciences, or related field3+ years of clinical SAS programming experience in pharma, biotech, or CROStrong command of Base SAS/SAS Macro; SAS/STAT a plusSolid working knowledge of CDISC SDTM and ADaM standardsExperience supporting regulatory submissions (NDA/BLA) a plusComfortable working with lean teams and evolving standards at a growing organization Disclosure: The hourly rates and/or salaries listed may or may not reflect total compensation packages including bonus and fringe benefits, etc., nor are the advertisement(s) posted a guarantee of a certain compensation package for a position or bona fide offer of employment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.