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Senior Statistical Programmer Jobs in Michigan (NOW HIRING)

Enwork

Senior Quality Engineer

Lowell, MI · On-site

$82K - $111K/yr

With the dynamic growth of Enwork, the Senior Quality Engineer position provides an opportunity to ... Related fields or experience is acceptable. • Technical Expertise: o Proficiency in statistical ...

Enwork

Senior Quality Engineer

Lowell, MI · On-site

$82K - $111K/yr

Description With the dynamic growth of Enwork, the Senior Quality Engineer position provides an ... Technical Expertise: o Proficiency in statistical analysis. o Proficiency with quality tools like ...

Aspen Surgical

Sr Packaging Engineer

Caledonia, MI · On-site

The Senior Packaging Engineer will drive packaging development, validation, and optimization ... Experience with statistical analysis tools (Minitab or equivalent) and TOPS (or similar system). We ...

Munich Re

Data Scientist, AI

Ann Arbor, MI · On-site +1

Proficiency in statistical programming languages such as R, Python, SAS, or similar, alongside ... * Sr. Data Scientist: 4 or more years of data science/predictive analytics experience in (re ...

Benesch

Senior Municipal Engineering

Detroit, MI · On-site

$103K - $142K/yr

Statistics show that women and underrepresented groups are less likely to apply for a position if ... Senior Project Engineer - Municipal Engineering Benesch has an exciting opportunity for a creative ...

Aptiv

Sr. Algorithm Engineer

Troy, MI · On-site

$99K - $136K/yr

Senior Algorithm Engineer Why join Aptiv? You'll have the opportunity to work on cutting-edge ... Knowledge of vehicle dynamics, numerical methods and statistic methods * Experience in code ...

Benesch

Senior Municipal Engineering

Detroit, MI · On-site

$103K - $142K/yr

Statistics show that women and underrepresented groups are less likely to apply for a position if ... Senior Project Engineer - Municipal Engineering Benesch has an exciting opportunity for a creative ...

Aptiv PLC

Sr. Algorithm Engineer

Troy, MI · On-site

$99K - $136K/yr

Senior Algorithm Engineer Why join Aptiv? You'll have the opportunity to work on cutting-edge ... Knowledge of vehicle dynamics, numerical methods and statistic methods * Experience in code ...

Aptiv

Sr. Algorithm Engineer

Troy, MI · On-site

$99K - $136K/yr

Senior Algorithm Engineer Why join Aptiv? You'll have the opportunity to work on cutting-edge ... Knowledge of vehicle dynamics, numerical methods and statistic methods * Experience in code ...

GM Financial

Sr Data Scientist

Detroit, MI · On-site

... statistical models in originations, collections, risk, pricing, fraud, customer experience and ... linear programming techniques. * Advanced skills in Python, SAS, SQL, R, JMP, Excel, Word ...

Pwc

US Tech - AI Engineering Senior Associate

Detroit, MI · On-site

$55K - $187K/yr

... Level Senior Associate & Summary At PwC, our people in data and analytics engineering focus on ... You will work on developing predictive models, conducting statistical analysis, and creating data ...

Aptiv

Sr. Algorithm Developer

Troy, MI · On-site

$51.75 - $68.50/hr

Senior Algorithm Engineer Why join Aptiv? You'll have the opportunity to work on cutting-edge ... Knowledge of vehicle dynamics, numerical methods and statistic methods * Experience in code ...

Aptiv

Sr. Algorithm Developer

Troy, MI

$51.75 - $68.25/hr

Senior Algorithm Engineer Why join Aptiv? You'll have the opportunity to work on cutting-edge ... Knowledge of vehicle dynamics, numerical methods and statistic methods * Experience in code ...

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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 13, 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:
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Senior Statistical Programmer jobs near you
Senior Biostatistician - Remote (US)

Senior Biostatistician - Remote (US)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Re-posted 2 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.
Senior Biostatistician:
Responsibilities:
  • Create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams.
  • Develop phase 1-4 SAPs and make significant contributions to iSAPs. Create SAP TLFs shells for all phases and studies.
  • Review ADAM and TLFs; work with client and programmers to resolve comments.
  • Strong programming and logic skills (working knowledge of SAS)
  • Ability to apply drug development knowledge during production of high quality statistical analyses.
  • Perform sample size calculations for a variety of scenarios and study designs.
  • Leads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor.
  • Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas.
  • Understand the various tools that we work with
  • High level knowledge of drug development as it pertains to biostatistics.
  • Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
  • Review the statistical section of a Sponsor's protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives. Provide valuable feedback to the Sponsor on the statistical aspects of the study. Create the statistical section of the Sponsor's protocol with minimal support
  • High proficiency with MS Office applications
  • Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation.
  • Provide ICH guideline based input as applicable to statistics.
  • Prepare and review statistical methods and results sections for the CSR with minimal support in collaboration with in-house medical writers.
Requirements:
  • College graduate in Biostatistics, Statistics, or Mathematics discipline or related field, masters or PhD preferred, or many years of related experience required.
  • Minimum of 5 years' experience in Biostatistics or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Has high level knowledge of drug development as it pertains to biostatistics; has the ability to apply drug development knowledge during production of high quality statistical analyses.
  • Strong SAS programming, SAS base, SAS macro experience.
  • Thorough knowledge and understanding of clinical data preferred.
  • Strong experience with data and production of TLGs.
  • Excellent scientific writing skills.
  • Strong resource for biostatistics; willing to guide others in a variety of biostatistical techniques.
  • 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 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.

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