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Senior Statistical Programmer Jobs in Colorado (NOW HIRING)

Ra

Marketing Analytics Senior Manager

Denver, CO · On-site

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

CPC Clinical Research

Senior Biostatistician

Aurora, CO · On-site

$120K - $150K/yr

Statistical Programming & Analysis * Develop, validate, or oversee statistical programming using SAS and other tools (e.g., R, Python). * Review outputs for accuracy, quality, and compliance with ...

CPC

Senior Biostatistician

Aurora, CO · On-site

Statistical Programming & Analysis * Develop, validate, or oversee statistical programming using SAS and other tools (e.g., R, Python). * Review outputs for accuracy, quality, and compliance with ...

Ra

Marketing Analytics Manager

Denver, CO

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 ...

Three Point Solutions, Inc.

Sr Process Engineer

Boulder, CO · On-site

$109K - $141K/yr

Job Title: Sr Process Engineer Client: Medical Device Manufacturing Company Duration: 2 Years ... statistical analysis and process performance evaluations • Ensure compliance with quality and ...

Three Point Solutions

Sr Process Engineer

Boulder, CO · On-site

$45 - $50/hr

Job Title: Sr Process Engineer Client: Medical Device Manufacturing Company Duration: 2 Years ... statistical analysis and process performance evaluations • Ensure compliance with quality and ...

Apply Early

Three Point Solutions

Sr Process Engineer

Boulder, CO · On-site

$48 - $50/hr

Job Title: Sr Process Engineer Client: Medical Device Manufacturing Company Location: Boulder, CO ... Perform statistical analysis * Ensure safety and product quality Top Technical Skills * Process ...

Apply Early

Hirsch Precision

Senior Calypso CMM Programmer

Longmont, CO · On-site

$105K - $130K/yr

Position Summary We are seeking a highly experienced Senior Calypso CMM Programmer with 15+ years ... Statistical analysis and SPC * MSA and Gage R&R * Excellent communication and cross-functional ...

Apply Early

CoorsTek

Global Process Engineer Sr

Golden, CO · On-site

$107K - $138K/yr

Job Title Global Process Engineer Sr As the Global Process Engineer Senior, you will be responsible ... Apply knowledge of statistical analysis, project management, Lean Six Sigma, quality, and basic ...

CoorsTek, Inc.

Global Process Engineer Sr

Golden, CO · On-site

$107K - $138K/yr

Job Title Global Process Engineer Sr As the Global Process Engineer Senior, you will be responsible ... Apply knowledge of statistical analysis, project management, Lean Six Sigma, quality, and basic ...

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All JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in Colorado

Senior Statistical Programmer information

See Colorado salary details

$86.8K

$134.9K

$176.1K

How much do senior statistical programmer jobs pay per year?

As of Jul 2, 2026, the average yearly pay for senior statistical programmer in Colorado is $134,903.00, according to ZipRecruiter salary data. Most workers in this role earn between $112,500.00 and $155,600.00 per year, depending on experience, location, and employer.

What is a Senior Statistical Programmer job?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the key skills and qualifications needed to thrive in the Senior Statistical Programmer position, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a Senior Statistical Programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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Senior Statistical Programmer jobs near you

Senior Statistical Programmer

Katalyst Healthcares and Life Sciences

Boulder, CO • On-site

Other

Posted 9 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
  • ssist 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.

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