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Entry Level Clinical Sas Programmer Jobs in Michigan

A2 Ai

Statistical Programmer

Ann Arbor, MI · On-site

$75 - $110/hr

Develop and maintain programming code using R and/or SAS to create, validate, and QC clinical datasets. * Perform quality control (QC) of datasets, programming outputs, and submission documentation ...

Delta Dental of Michigan

Data Scientist

Okemos, MI · On-site

Knowledge of health or dental insurance, or of dental clinical practice preferred. Position ... SAS, R, or equivalent preferred; experience with programming languages, especially Python and SQL ...

Delta Dental of Michigan

Data Scientist

Okemos, MI · Hybrid

Knowledge of health or dental insurance, or of dental clinical practice preferred. Position ... SAS, R, or equivalent preferred; experience with programming languages, especially Python and SQL ...

LEARN Behavioral

Board Certified Behavior Analyst

Okemos, MI · On-site

$67K - $82K/yr

Senior Behavior Specialist (Grad students or new grads pursuing supervision hours) * Entry-Level ... Monthly clinical forums (live CEUs) * Person-centered care and assent-based treatment programming

LEARN Behavioral

Board Certified Behavior Analyst

Okemos, MI · On-site

$67K - $82K/yr

Senior Behavior Specialist (Grad students or new grads pursuing supervision hours) * Entry-Level ... Monthly clinical forums (live CEUs) * Person-centered care and assent-based treatment programming

LEARN Behavioral

Board Certified Behavior Analyst

Okemos, MI · On-site

$67K - $82K/yr

Senior Behavior Specialist (Grad students or new grads pursuing supervision hours) * Entry-Level ... Monthly clinical forums (live CEUs) * Person-centered care and assent-based treatment programming

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Entry Level Clinical Sas Programmer information

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How much do entry level clinical sas programmer jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for entry level clinical sas programmer in Michigan is $47.10, according to ZipRecruiter salary data. Most workers in this role earn between $36.25 and $59.28 per hour, depending on experience, location, and employer.

What is an entry level clinical SAS programmer?

An Entry Level Clinical SAS Programmer is responsible for programming and analyzing clinical trial data using SAS software. They assist in creating datasets, reports, and statistical outputs that comply with regulatory standards. Their work supports biostatisticians and clinical teams in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role requires knowledge of SAS programming, clinical research processes, and regulatory requirements such as CDISC standards. It is an excellent starting point for those looking to build a career in clinical data analysis and biostatistics.

What are the typical responsibilities of an entry level clinical SAS programmer?

Entry Level Clinical SAS Programmers are primarily responsible for writing and validating SAS code to process clinical trial data, generate tables, listings, and figures, and support statistical analysis plans. They work closely with biostatisticians, data managers, and other team members to ensure data integrity and compliance with regulatory standards. Daily tasks may involve data cleaning, programming data checks, and documenting code for reproducibility. This role offers great exposure to the clinical data lifecycle and provides a strong foundation for professional growth within clinical research and data analytics.

What are the key skills and qualifications needed to thrive as an entry level clinical SAS programmer?

To thrive as an Entry Level Clinical SAS Programmer, you need a solid understanding of SAS programming, statistics, and clinical trial processes, often supported by a degree in computer science, statistics, or a related field. Familiarity with SAS software, data management systems, and FDA or CDISC standards is highly valued, and SAS certification can be a plus. Attention to detail, strong problem-solving skills, and effective communication are key soft skills for this role. These competencies ensure high-quality data analysis, regulatory compliance, and clear collaboration across teams in pharmaceutical or clinical research settings.

What are the most commonly searched types of Clinical Sas Programmer jobs in Michigan?

The most popular types of Clinical Sas Programmer jobs in Michigan are:

What are popular job titles related to Entry Level Clinical Sas Programmer jobs in Michigan?

For Entry Level Clinical Sas Programmer jobs in Michigan, the most frequently searched job titles are:

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Entry Level Clinical Sas Programmer jobs near you
Infographic showing various Entry Level Clinical Sas Programmer job openings in Michigan as of August 2026, with employment types broken down into 73% Full Time, and 27% Part Time. Highlights an 73% In-person, 18% Hybrid, and 9% Remote job distribution, with an average salary of $97,966 per year, or $47.1 per hour.

Statistical Programmer

A2 Ai

Ann Arbor, MI • On-site

$75 - $110/hr

Other

Posted 9 days ago

Job description

  • Generate and validate CDISC SDTM and ADaM datasets related to noncompartmental analysis (NCA), including PC/PP, ADPC, ADPP, and other relevant domains.
  • Develop submission-ready datasets that comply with CDISC standards, implementation guides, and controlled terminology.
  • Perform dataset validation using Pinnacle 21 (Community and/or Enterprise) and resolve validation findings to ensure regulatory compliance.
  • Prepare and maintain Define-XML packages and supporting metadata for regulatory submissions.
  • Develop and maintain programming code using R and/or SAS to create, validate, and QC clinical datasets.
  • Perform quality control (QC) of datasets, programming outputs, and submission documentation to ensure accuracy, completeness, and consistency with source data.
  • Support regulatory submissions to agencies such as the FDA, PMDA, and EMA by producing high-quality, submission-ready datasets and documentation.
Requirements
  • Bachelor’s degree in quantitative sciences, biostatistics, statistics, engineering, data science, or similar field. Master’s degree preferred.
  • Experience generating and validating CDISC SDTM and ADaM NCA domains (e.g., PC/PP, ADPC, ADPP, and related datasets).
  • Proficiency with Pinnacle 21 (Community and/or Enterprise) for validation.
  • Proficiency with R or SAS.
  • Experience preparing or reviewing Define-XML (define packages) for regulatory submissions.
  • Strong understanding of CDISC standards, controlled terminology, and implementation guides.
  • Experience supporting regulatory submissions (FDA, PMDA, or EMA) is preferred.
  • Strong attention to detail and ability to work independently in a collaborative environment.
  • This position is ideal for someone with hands-on experience in clinical data standards who can efficiently produce submission-ready datasets and associated documentation for NCA analyses.
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