Katalyst CRO

Senior Programmer

17 days ago

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Responsibilities

Develop and perform SAS programming for data processing and analysis.
Collaborate with statisticians and other programmers to ensure accuracy, consistency, and adherence to quality control (QC) procedures.
Support study deliverables and manage timelines for statistical data analysis and reporting.
Document and track programming differences between developers and Statistical QC programmers.
Provide programming support for ISS/Client and post-submission activities.
Ensure programming outputs align with industry standards and project expectations.
Maintain up-to-date documentation for all study-related programming tasks.
Develop, program, test, and maintain validation/edit checks in SAS.
Perform peer programming validation to ensure quality and consistency.
Offer technical expertise and support to the Data Management team.
Participate in study setup, database lock activities, and team meetings.
Manage project priorities and timelines efficiently.
Apply knowledge of statistical terminology, clinical data structures, regulatory standards, and protocol designs.

Requirements:

Bachelor's degree in Biostatistics, Mathematics, Computer Science, or a relevant scientific discipline.
5+ years of SAS programming experience in the pharmaceutical, biotech, or CRO industry (Oncology experience preferred).
Strong SAS programming, macro development, and SAS graphing skills.
Experience with CDISC standards (CDASH/SDTM/ADaM).
Familiarity with ISS (Integrated Summary of Safety) and Client (Integrated Summary of Efficacy) is a plus.
SAS Certification (Base Programmer for SAS 9 or Advanced Programmer for SAS 9) preferred.
Strong analytical and problem-solving abilities.
Excellent oral and written communication skills for cross-functional collaboration.
Detail-oriented, dependable, and self-motivated.