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 ...

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 ...
Sr.Statistical Programmer
Boulder, CO · On-site
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 ...
Sr.Statistical Programmer
Boulder, CO · On-site
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 ...
Sr. Statistical Programmer
Baltimore, MD · On-site
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 ...
Sr. Statistical Programmer
Baltimore, MD · On-site
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 ...
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 ...
Sr. Statistical Programmer
Omaha, NE · On-site
Maintains a basic understanding of relevant industry trends in standards implementation, clinical statistical programming, and ophthalmology * Provides technical consultation and collaborates with ...
Sr. Statistical Programmer
Omaha, NE · On-site
Maintains a basic understanding of relevant industry trends in standards implementation, clinical statistical programming, and ophthalmology * Provides technical consultation and collaborates with ...
Senior Statistical Programmer
Boulder, CO · 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 ...
Senior Statistical Programmer
Boulder, CO · 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 ...
Senior Statistical Programmer
Austin, TX · 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 ...
Senior Statistical Programmer
Austin, TX · 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 ...
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 ...
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 ...
We are seeking a highly skilled Sr. Engineer - Process Development (CQV) to support automated and semi-automated combination product assembly, labeling, and packaging operations within a GMP Final ...
We are seeking a highly skilled Sr. Engineer - Process Development (CQV) to support automated and semi-automated combination product assembly, labeling, and packaging operations within a GMP Final ...
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 Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
Sr.Statistical Programmer
Boulder, CO · On-site
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 ...
Sr.Statistical Programmer
Boulder, CO · On-site
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 ...
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 ...
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 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 ...
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 ...
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 ...
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 ...
Senior Statistical Programmer
Dunkirk, NY · On-site
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 ...
Senior Statistical Programmer
Dunkirk, NY · On-site
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 ...
Senior Statistical Programmer
Dunkirk, NY · On-site
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 ...
Senior Statistical Programmer
Dunkirk, NY · On-site
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 ...
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 ...
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 ...
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 ...
Katalyst Jobs Information
What is it like to work at Katalyst?
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
What makes Katalyst an attractive place to work?

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.
- 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.