Katalyst
Katalyst

61 Katalyst Senior Statistical Programmer Jobs Hiring Near You

The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...

The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...

The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...

The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials * This role is key to implementing ...

Maintains a basic understanding of relevant industry trends in standards implementation, clinical statistical programming, and ophthalmology * Provides technical consultation and collaborates with ...

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 ...

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 ...

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 ...

The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory ...

The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables ...

Position Summary A Senior Statistical Programming is an expert in the management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ...

The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables ...

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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.
What other companies are hiring for Senior Statistical Programmer jobs?
Infographic showing various Senior Statistical Programmer job openings at Katalyst in the United States as of August 2026, with employment types broken down into 99% Full Time, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution.

Senior Statistical Programmer

Katalyst

Lake Villa, IL • On-site

Full-time

Re-posted yesterday


Job description

Job Description:
  • We are seeking a highly motivated and qualified individual to join our Clinical Department as a Senior Statistical Programmer and work as part of a team to drive success.
  • Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team.
  • The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses.
  • This position requires close collaboration with cross-functional teams to ensure the integrity and accuracy of clinical data used in regulatory filings and internal reporting.

Responsibilities:
  • Independently develop, validate, document and troubleshoot SAS programs for the preparation of periodic internal reports, regulatory submissions, and ad hoc analyses.
  • Create and maintain analysis and submission datasets (ADaM, SDTM) in compliance with CDISC standards and regulatory guidance.
  • Design, develop, validate, update, and document SAS programs to generate analysis datasets, data listings, tables, and graphs of high quality in a timely manner.
  • Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies,
  • Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
  • Develop software tools, SAS macros and utilities to automate programming activities and improve programming efficiency and quality.
  • Create SAS macros or other tools to enhance the efficient delivery of statistical services, providing associated documentation and staff training as needed.
  • Program quality checks for clinical study raw data and report findings.
  • Review or author SDTM and ADaM specifications and datasets.
  • Manage CROs, including reviewing or validating statistical deliverables of vendors.
  • Provides input in the design and development of case report forms.
  • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience.
  • Establish and maintain excellent working relationships with critical collaborative partners throughout the company.
Requirements:
  • Bachelor's degree in Biostatistics, Mathematics, Statistics, Computer Science, or related field
  • Minimum 6 years' experience in bio-pharma statistical programming
  • Advanced SAS programming skills in SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL with a demonstrated mastery of SAS/STAT procedures
  • Strong expertise in CDISC including SDTM, ADaM, and CDASH
  • Extensive experience in SAS macro functions and dynamic code generations.
  • Experience in regulatory submissions (e.g., NDAs and DSURs)
  • High attention to detail, with a focus on quality and traceability in all deliverables
  • Strong interpersonal and teamwork skills with a collaborative mindset and the ability to manage multiple priorities in a fast-paced and dynamic environment with shifting timelines and evolving needs
  • Take initiatives to solve problems proactively and think critically
  • Willing to adapt to changing business needs, able to pivot between tasks
  • Able to make complex programming and data-related decisions independently
  • Comprehensive knowledge and deep understanding of statistical programming environments, processes, procedures, and roles for clinical development from Phase 1 through regulatory submission
  • Up to date with CDISC standards, industry trends, best practices, and statistical programming methodology.