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Join to apply for the Sr SAS Programmer role at Katalyst CRO . This position supports the Biostatistics team by carrying out programming activities, overseeing external vendors, and ensuring timely and accurate programming and validation activities for clinical studies and publications. Responsibilities include: Supporting programming activities for clinical studies, overseeing external vendors, and ensuring quality and timeliness. Contributing to the efficiency and best practices of the Biostatistics group. Providing statistical programming and validation support for clinical reports, overseeing vendor activities, and coordinating programming efforts. Working with data formats like SDTM, ADaM, and converting data from various sources. Collaborating with clinicians, statisticians, and publication teams to generate and QC outputs, review publications, and coordinate resources. Developing statistical analysis plans, datasets, validation plans, and maintaining programming standards. Working independently and proposing improvements to programming processes. Requirements: Bachelor's degree in a related science discipline. 7+ years of SAS programming experience in a clinical trial environment. Proficiency in SAS (Base, MACRO, STAT, GRAPH, ACCESS), MS Office, and familiarity with Unix/Windows. Experience with CDISC standards (SDTM, ADaM). Understanding of FDA guidelines and software development lifecycle. Strong organizational, communication, and problem-solving skills. 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