Clinical SAS Programmer
About the position Responsibilities • Develop, test, and validate SAS programs for clinical trial data analysis and reporting. • Generate and QC tables, listings, and figures (TLFs) for clinical study reports. • Provide programming support for data management, data review, and ad hoc analyses. • Ensure compliance with regulatory requirements (e.g., FDA, EMA) and company standards. • Participate in the creation of submission documentation for regulatory filings. • Collaborate with statisticians and other team members to ensure timely and accurate delivery of high-quality datasets and outputs. • Perform programming and validation of data integration and data mapping as necessary. Requirements • Bachelor's degree in Computer Science, Statistics, Mathematics, or a related field; advanced degree preferred. • At least 3 years of experience as a SAS programmer in the pharmaceutical or biotechnology industry. • Strong experience with SAS programming (data step, PROC SQL, macros, and statistical procedures). • Demonstrated experience with Pinnacle 21 and submissions to regulatory authorities. • Knowledge of CDISC standards (SDTM, ADaM) and regulatory submission requirements. • Excellent problem-solving skills and attention to detail. • Strong communication and collaboration abilities. Nice-to-haves • Exposure to clinical trials in rare diseases. • Experience with other programming languages (e.g., R, Python). • Familiarity with clinical data management systems (e.g., Medidata Rave, Oracle Clinical). Benefits • Voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. • Access to a retirement savings plan. • Service bonus and holiday pay plans (earn up to eight paid holidays per benefit year). • Transit spending account. • Paid sick leave under the applicable state or local plan. Apply tot his job