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62 Katalyst Senior Statistical Programmer Jobs Hiring Near You

Katalyst

Sr. Statistical Programmer

Cincinnati, OH · On-site

Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...

Katalyst

Sr. Statistical Programmer

Boulder, CO · Remote

Act as primary programming contact for assigned studies, collaborating closely with statisticians, data managers, and medical writers in a fully remote, fast-paced environment. * Conduct independent ...

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are ...

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Katalyst Jobs Information

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Katalyst is a forward-thinking company that has established itself as a leader in its industry, known for its commitment to innovation and customer satisfaction. The company's work environment is characterized by a collaborative and dynamic atmosphere, where employees are encouraged to share ideas and work together to drive progress. Joining Katalyst offers opportunities for professional growth and development, as well as the chance to contribute to meaningful projects that can have a lasting impact.

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Infographic showing various Senior Statistical Programmer job openings at Katalyst in the United States as of August 2026, with employment types broken down into 98% Full Time, and 2% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Sr. Statistical Programmer

Katalyst

Cincinnati, OH • On-site

Full-time

Re-posted 5 days ago

Job description

Responsibilities:
  • Ensure departmental or functional training plans in place and appropriate
  • Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget
  • Generate, validate, and/or review SDTM domains and ADaM datasets and associated specifications
  • Generate, validate, and/or review tables, figures and listings to support the statistical analysis of clinical trials data in support of regulatory submissions and publications
  • Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports)
  • Maintain complete and auditable documentation of all programming activities
  • Manage datasets and output across SAS programs, studies, and indications to ensure consistency
  • Manage and provide statistical programming support to supplemental or exploratory analyses for pharmacovigilance, regulatory agencies, or any other internal and external ad-hoc requests
  • Manage programming, testing, and documenting SAS global utility programs and tools in accordance with standards and validation procedures
  • Develop and/or maintain departmental procedures and standards
  • Review CRFs, edit check specifications, and table, figure, and listing mock-ups
  • Manage, generate, and/or review acrf.pdf, define.xml, define.pdf, and reviewer's guide documents
  • Assist in validation of SAS per 21 CFR Part 11
  • Train and mentor new members and programmers; supervise contract programmers, as needed
Requirements:
  • Bachelor's degree in Statistics, Mathematics, Computer Science or a related field required
  • Minimum of 6 years biotechnology/pharmaceutical/CRO industry experience as a statistical programmer
  • Prior experience overseeing statistical programming contractors required
  • Compound oversight experience highly preferred
  • Extensive knowledge of SAS Macros highly preferred, in addition to knowledge of Base SAS, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS
  • Experience working with other languages or software (R, Python, Spotfire) in validated environments is strongly preferred
  • Demonstrates extensive knowledge with industry standards, such as the ICH guidelines, CDISC standards/implementation guides, 21 CFR Part 11, and FDA guidelines
  • eCTD NDA submission experience is a must.

Apply