ZipRecruiter

Log In

1

Clinical Statistical Programmer Jobs in Colorado

CPC Clinical Research

Senior Biostatistician

Aurora, CO · On-site

$120K - $150K/yr

PhD or Master's degree in Biostatistics, Statistics, or related field with at least 5 years of experience in clinical trial data analysis * Demonstrated programming proficiency in SAS (version 9.0 or ...

CPC

Senior Biostatistician

Aurora, CO

PhD or Master's degree in Biostatistics, Statistics, or related field with at least 5 years of experience in clinical trial data analysis * Demonstrated programming proficiency in SAS (version 9.0 or ...

Vizient

Lead Data Scientist

Englewood, CO · On-site

... clinical, operational, and economic outcomes. You will influence technical strategy, drive ... Partner with engineering, platform, and business teams to deploy, monitor, and maintain production ...

Vizient, Inc.

Lead Data Scientist

Centennial, CO · On-site

... clinical, operational, and economic outcomes. You will influence technical strategy, drive ... Partner with engineering, platform, and business teams to deploy, monitor, and maintain production ...

next page

Showing results 1-20

All JobsClinical Statistical Programmer JobsClinical Statistical Programmer Jobs in Colorado

Clinical Statistical Programmer information

See Colorado salary details

$17

$56

$94

How much do clinical statistical programmer jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for clinical statistical programmer in Colorado is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $36.15 and $85.67 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Statistical Programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are the key skills and qualifications needed to thrive as a Clinical Statistical Programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What does a Clinical Statistical Programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What Does a Clinical Statistical Programmer Do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

More about Clinical Statistical Programmer jobs
What are popular job titles related to Clinical Statistical Programmer jobs in Colorado? For Clinical Statistical Programmer jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Clinical Statistical Programmer jobs in Colorado look for? The top searched job categories for Clinical Statistical Programmer jobs in Colorado are:
What are popular job titles related to Clinical Statistical Programmer jobs in CO? For Clinical Statistical Programmer jobs in CO, the most frequently searched job titles are:
Clinical Statistical Programmer jobs near you
Senior Biostatistician

Senior Biostatistician

CPC Clinical Research

Aurora, CO • On-site

$120K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

Key Responsibilities
Leadership & Project Oversight
  • Serve as the lead biostatistician on clinical study teams, accountable for statistical deliverables, quality, and timelines.
  • Provide mentorship and oversight to statisticians and statistical programmers.
  • Communicate project progress, risks, and resource needs to leadership.
  • Ensure alignment of project execution with departmental and organizational goals.

Study Design & Statistical Strategy
  • Lead the statistical design of clinical studies, including protocol development and statistical methodologies.
  • Perform and review sample size and power calculations.
  • Develop, review, and finalize statistical analysis plans (SAPs).
  • Recommend innovative statistical approaches, endpoints, and reporting strategies aligned with study objectives.

Data Management & Systems Collaboration
  • Provide statistical input into electronic data capture (EDC) design.
  • Partner with data management to define edit checks and ensure high-quality data collection.
  • Ensure study data supports interim and final analyses and regulatory requirements.

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 standards.
  • Guide programming specifications, table shells, and reporting frameworks.

Reporting & Scientific Communication
  • Lead preparation and review of interim analyses, final study reports, and regulatory submissions.
  • Contribute to manuscripts, abstracts, integrated summaries, and ad hoc analyses.
  • Communicate complex statistical concepts and results to non-statistical stakeholders and senior leadership.

Regulatory Compliance & Quality Assurance
  • Ensure compliance with GCP, FDA, ICH, and other applicable regulatory standards.
  • Maintain audit-ready documentation and high-quality, submission-ready deliverables.
  • Contribute to the development and refinement of statistical SOPs and best practices.

Collaboration & Stakeholder Engagement
  • Collaborate with clinical operations, data management, physicians, and external partners.
  • Interface with regulatory agencies, data monitoring committees, and steering committees.
  • Build strong client relationships and support business development initiatives.

Specialized & Strategic Contributions
  • Provide statistical consulting across therapeutic and technical domains.
  • Support specialized activities such as randomization design, unblinded statistician roles, and integrated summaries of safety and efficacy.
  • Represent the organization through publications, conference participation, and professional engagement.

Qualifications
Required
  • PhD or Master's degree in Biostatistics, Statistics, or related field with at least 5 years of experience in clinical trial data analysis
  • Demonstrated programming proficiency in SAS (version 9.0 or higher)
  • Experience supporting Phase I-III clinical trials
  • Strong knowledge of ICH guidelines and regulatory requirements; familiarity with FDA submission processes
  • Familiarity with CDISC standards (e.g., SDTM, ADaM) for regulatory submissions
  • Proven leadership experience managing projects and mentoring team members
  • Proficiency with Microsoft Office tools (Word, Excel, PowerPoint)
  • Experience working on integrated summaries of safety and efficacy (ISS/ISE) or similar large-scale reporting efforts
  • Strong analytical, organizational, and problem-solving skills with high attention to detail
  • Excellent communication and interpersonal skills, with the ability to convey complex statistical concepts clearly
  • Ability to manage multiple trials and priorities simultaneously with minimal disruption to productivity

Preferred
  • Experience with FDA/NDA submissions and regulatory interactions
  • Experience working in a client-facing or CRO environment
  • Therapeutic area expertise
  • Proficiency in R, Python, or other advanced analytical tools
  • Track record of contributions to publications, abstracts, or conference presentations

Posting deadline: This posting will remain open until filled. For best consideration, please apply by July 1, 2026.
Note: Viable applicants will be required to pass a background and education verification check.
About CPC:
CPC is an academic research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 30 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more.
CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.
CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. http://www.cpccommunityhealth.org/
CPC offers:
  • Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
  • Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)
  • 11 paid holidays
  • 15 - 25 vacation days based on years of service
  • Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours)
  • Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)
  • Flexible and remote work schedules

An Equal Opportunity Employer
CPC is dedicated to the principles of equal employment opportunity (EEO). CPC prohibits unlawful discrimination against applicants or employees on the basis of age 40 and over, race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, sexual orientation, gender identity, gender expression, color, religion, creed, national origin, ancestry, disability, military status, genetic information, marital status, or any other status protected by applicable state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.
Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at careers@cpcmed.org.

Apply