Katalyst CRO
Join to apply for the Clinical Statistical Programmer - III role at Katalyst CRO . This job was posted 8 months ago. Get AI-powered advice on this job and more exclusive features. Responsibilities Provide programming support for study deliverables, ensuring timelines and quality standards are met. Collaborate with Data Management and Biostatistics teams on database and dataset specifications, timelines, and quality requirements. Create and validate SDTM and ADaM datasets and submission deliverables in compliance with industry standards and project-specific requirements. Create and validate TFL outputs according to study requirements. Receive, import, and verify external data structures. Create and maintain supporting documentation. Requirements B.S. or equivalent in computer science, mathematics, or life sciences. At least 5 years of clinical research programming experience, with 3 years in the pharmaceutical industry. Experience in analysis and reporting of phase I-IV clinical trial data. Proficiency in SAS/Base and SAS/Stat. Knowledge of CDISC standards: CDASH, SDTM, ADaM, DEFINE-XML, and Controlled Terminology. Additional Details Seniority level: Associate Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting is still active. No indication that it is expired. #J-18808-Ljbffr