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Senior Manager Statistical Programming Jobs in Illinois

cap

Senior SAS Programmer

Winnetka, IL · Remote

$87K - $111K/yr

The validity of statistical programming used in assigned projects. * Provide timely and accurate ... Other assignments as directed by the Manager. Knowledge / Skills Required / Preferred Personal:

InterSources

SAS / Statistical Programmer

Chicago, IL · On-site

... Data Management on edit checks etc is preferred. Good knowledge of statistical programming languages (including SAS). About InterSources Inc: InterSources Inc, a Certified Diverse Supplier, was ...

Ra

Marketing Analytics Manager

Chicago, IL

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Capital One

Sr. Manager, Product Management

Chicago, IL · On-site

$130.30K - $172K/yr

A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics ... Engineering, Information Systems or a related quantitative field) * A Master's Degree in a ...

Capital One

Sr. Manager, Product Management

Riverwoods, IL · On-site

$131.30K - $173.40K/yr

A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics ... Engineering, Information Systems or a related quantitative field) * A Master's Degree in a ...

Capital One

Sr. Manager, Product Management

Chicago, IL · On-site

$130.30K - $172K/yr

A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics ... Engineering, Information Systems or a related quantitative field) * A Master's Degree in a ...

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Senior Manager Statistical Programming information

What are the key skills and qualifications needed to thrive as a Senior Manager Statistical Programming, and why are they important?

To thrive as a Senior Manager Statistical Programming, you need expertise in biostatistics, programming languages like SAS or R, and experience with clinical trial data, typically supported by an advanced degree in a quantitative field. Familiarity with regulatory requirements (e.g., CDISC standards), clinical data management systems, and project management tools is essential. Strong leadership, communication, and problem-solving skills help you lead teams and liaise with cross-functional stakeholders. These skills ensure accurate, compliant data analyses and effective team management for successful clinical trial outcomes.

How does a Senior Manager Statistical Programming typically collaborate with cross-functional teams in clinical research projects?

A Senior Manager Statistical Programming plays a pivotal role in coordinating with biostatisticians, clinical data managers, and medical writers to ensure seamless data flow and analysis throughout clinical trials. They oversee programming teams to deliver statistical outputs, such as tables, listings, and figures, while maintaining compliance with regulatory standards. Regular meetings and clear communication are essential, as the Senior Manager must interpret project requirements and translate them into actionable programming tasks, ensuring timelines and quality standards are met. This collaborative environment fosters continuous learning and problem-solving, as cross-functional input is vital for addressing complex data challenges.

What are Senior Manager Statistical Programming?

A Senior Manager Statistical Programming is a leadership role in the field of clinical research and biostatistics, typically within the pharmaceutical, biotechnology, or contract research organization (CRO) industries. This professional oversees teams of statistical programmers responsible for analyzing clinical trial data, ensuring data accuracy, and delivering high-quality statistical outputs for regulatory submissions. The role involves project management, resource allocation, mentoring staff, and collaborating with cross-functional teams to ensure compliance with regulatory standards and timelines.

What is the difference between Senior Manager Statistical Programming vs Statistical Programmer?

AspectSenior Manager Statistical ProgrammingStatistical Programmer
CredentialsBachelor's/Master's in Biostatistics, Computer Science, or related field; often with management experienceBachelor's or Master's in Biostatistics, Statistics, or related field
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms data analysis, programming, and validation tasks under supervision
Employer & Industry UsagePharmaceutical, biotech companies, CROs, clinical researchPharmaceutical, biotech, clinical research organizations

The main difference is that Senior Manager Statistical Programming oversees teams and manages projects, while Statistical Programmers focus on executing data analysis and programming tasks. The senior role involves leadership responsibilities, whereas the programmer role is more technical and task-oriented.

What are the most commonly searched types of Senior Statistical Programming jobs in Illinois? The most popular types of Senior Statistical Programming jobs in Illinois are:
What are popular job titles related to Senior Manager Statistical Programming jobs in Illinois? For Senior Manager Statistical Programming jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Senior Manager Statistical Programming jobs in Illinois look for? The top searched job categories for Senior Manager Statistical Programming jobs in Illinois are:
What cities in Illinois are hiring for Senior Manager Statistical Programming jobs? Cities in Illinois with the most Senior Manager Statistical Programming job openings:
Senior Manager Statistical Programming jobs near you
Infographic showing various Senior Manager Statistical Programming job openings in Illinois as of May 2026, with employment types broken down into 65% Full Time, 27% Part Time, and 8% Contract. Highlights an 97% Physical, 2% Hybrid, and 1% Remote job distribution.
Senior Statistical Programmer

Senior Statistical Programmer

Katalyst HealthCares & Life Sciences

Antioch, IL • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Senior Statistical Programmer

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.
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About Katalyst Healthcares & Life Sciences

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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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