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Senior Statistical Programmer Jobs in Michigan (NOW HIRING)

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 ...

Sr Quality Engineer

Muskegon, MI

$81K - $110K/yr

The Senior Quality Engineer is a senior professional that is responsible for ensuring that our ... Perform statistical analysis and review data trends to ensure that materials and products comply ...

Senior Systems Engineer

Lansing, MI · On-site

$106K - $145K/yr

We are seeking a Senior Systems Engineer to join our team. This role will involve supporting ... Application of statistical concepts to support data analysis, performance measurement, and ...

Sr Quality Engineer

Muskegon, MI · On-site

$80K - $108K/yr

Description The Senior Quality Engineer is a senior professional that is responsible for ensuring ... Perform statistical analysis and review data trends to ensure that materials and products comply ...

Senior Software Engineer - Prediction

Detroit, MI · On-site

$121K - $159K/yr

Latitude AI develops automated driving technologies and is seeking a Senior Software Engineer ... the statistical properties and quality of predictions and plans • Build a system that safely ...

Senior Systems Engineer

Lansing, MI · On-site

$106K - $145K/yr

Job Title: Senior Systems Engineer Location: Lansing MI Duration: 12 Months ( Hybrid Role) This ... Azure Statistics Audits & security plans Federal requirements - NIST 800-53, IRS Pub 1075, SSA ...

Senior Cloud Database Engineer

Dearborn, MI

$97K - $132K/yr

Senior Cloud Database Engineer #1059226 * We are seeking a Senior Cloud Database Engineer with 5+ ... Partner with AI/ML teams to embed ML, statistical models, and GenAI into data platform strategies.

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... Statistics - Demonstrating proficiency in data engineering platforms like Databricks - Utilizing ...

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Senior Statistical Programmer information

See Michigan salary details

$71.9K

$111.8K

$146K

How much do senior statistical programmer jobs pay per year?

As of Jul 9, 2026, the average yearly pay for senior statistical programmer in Michigan is $111,820.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,300.00 and $129,000.00 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.

What are the most commonly searched types of Statistical Programmer jobs in Michigan? The most popular types of Statistical Programmer jobs in Michigan are:
What are popular job titles related to Senior Statistical Programmer jobs in Michigan? For Senior Statistical Programmer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Senior Statistical Programmer jobs in Michigan look for? The top searched job categories for Senior Statistical Programmer jobs in Michigan are:
What cities in Michigan are hiring for Senior Statistical Programmer jobs? Cities in Michigan with the most Senior Statistical Programmer job openings:
Senior Statistical Programmer - Remote

Senior Statistical Programmer - Remote

MMS

Canton, MI • On-site

Full-time

Re-posted 7 days ago


Job description

About MMS
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Applicants must be legally authorized to work in the U.S. for any employer; we cannot sponsor visas (e.g., H-1B) or offer work authorization transfers at this time.
Job Specific Skills:
  • Mastery and trained on generating tables, listings, and graphs from clinical trial databases using SAS.
  • Utilizes System Development Life Cycle (SDLC) for programming deliverables.
  • Advanced user in SAS programming, SAS Base, and SAS Macros.
  • Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
  • Mastery and trained on SDTM standards including ability to write specifications.
  • Advanced knowledge of ADaM standards including supporting specification writing.
  • Proficient with MS Office applications.
  • Advanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements.
  • Advanced experience with pooling of data sets for submissions.
  • Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP.
  • Lead study or small programming project teams.
Job Requirements:
  • Masters required for all Statistics roles.
  • Minimum of 5 years’ experience in Statistical Programming or similar field required.
  • Expert knowledge of scientific principles and concepts. 
  • Reputation as emerging leader in field with sustained performance and accomplishment.
  • Proficiency with MS Office applications. 
  • Hands-on experience with clinical trial and pharmaceutical development preferred.   
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems. 
  • Excellent problem-solving skills. 
  • Good organizational and communication skills. 
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.  
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.  

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M. M. S. logo

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980