Principal Statistical Programmer

Join to apply for the Principal Statistical Programmer role at Katalyst CRO . Get AI-powered advice on this job and more exclusive features. Responsibilities Proficiency in CDISC standards (SDTM & Adam): Generate and validate datasets, create tables, listings, and figures (TLFs). Manage multiple projects as a Study Lead. Create and review submission documents and electronic case report forms (CRFs). Communicate effectively with cross-functional teams and clients. Support the Senior Director of Biometrics with statistical consultation, analysis plans, data review, and programming of SAS datasets. Develop programming specifications and support data integration across studies. Ensure timely and secure data and statistical reporting, participate in meetings, and assist with financial tracking and SOP development. Contribute to study support, training, and additional tasks as needed. Requirements MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field. At least 8 years (BS) or 6 years (MS or higher) of SAS programming experience in clinical trials. Knowledge of CDISC standards, SAS programming, and familiarity with other languages like R or Python is preferred. Understanding of clinical development and regulatory requirements is a plus. Additional Details Seniority level: Mid-Senior level Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting is active and not expired. #J-18808-Ljbffr