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Clinical Database Programmer Jobs in Michigan (NOW HIRING)

MMS

Senior Statistical Programmer - Remote

Canton, MI · On-site

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 ...

Zimmer Biomet

$13.75 - $18.50/hr

Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ... Basic understanding of relational databases and familiarity with writing or reading simple SQL ...

Zimmer Biomet

$13.75 - $18.50/hr

Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ... Basic understanding of relational databases and familiarity with writing or reading simple SQL ...

Zimmer Biomet

$13 - $17.50/hr

Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ... Basic understanding of relational databases and familiarity with writing or reading simple SQL ...

Zimmer Biomet

$14 - $18.50/hr

Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ... Basic understanding of relational databases and familiarity with writing or reading simple SQL ...

Zimmer Biomet

$14.75 - $19.50/hr

Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ... Basic understanding of relational databases and familiarity with writing or reading simple SQL ...

Zimmer Biomet

$14.50 - $19.25/hr

Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ... Basic understanding of relational databases and familiarity with writing or reading simple SQL ...

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All JobsClinical Database Programmer JobsClinical Database Programmer Jobs in Michigan

Clinical Database Programmer information

See Michigan salary details

$60.6K

$103.7K

$184.8K

How much do clinical database programmer jobs pay per year?

As of Jul 26, 2026, the average yearly pay for clinical database programmer in Michigan is $103,687.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,700.00 and $156,900.00 per year, depending on experience, location, and employer.

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

To excel as a Clinical Database Programmer, you need a bachelor's degree in computer science or a related field, experience in database design, and a strong understanding of clinical data standards. Proficiency in database management systems (such as Oracle or SQL), knowledge of electronic data capture (EDC) tools like Medidata Rave, and familiarity with programming languages like SAS or SQL are commonly required, along with certifications such as CDISC or Medidata Solutions. Attention to detail, problem-solving ability, and strong communication skills are valuable soft skills for this role. Mastering these competencies is vital for ensuring high-quality, regulatory-compliant clinical trial data and effective collaboration within multidisciplinary research teams.

What is a Clinical Database Programmer job?

A Clinical Database Programmer is responsible for designing, developing, and maintaining databases used in clinical trials. They ensure that data is collected, stored, and managed efficiently while complying with regulatory standards such as CDISC and FDA guidelines. Their role involves creating database structures, writing validation checks, and supporting data analysis to ensure accurate and reliable clinical trial results. They often work with clinical data managers, biostatisticians, and regulatory teams.

What are common responsibilities and team interactions for a Clinical Database Programmer in a typical workweek?

As a Clinical Database Programmer, your primary responsibilities usually include designing, building, and validating clinical trial databases, ensuring data is collected and managed in compliance with industry standards and regulatory requirements. You will frequently collaborate with clinical data managers, biostatisticians, and study coordinators to define data collection requirements and resolve data discrepancies. Team meetings and cross-functional communication are integral parts of the role, as you work together to maintain database integrity throughout the study lifecycle. This collaborative environment provides valuable experience in both technical problem-solving and teamwork, often paving the way for advancement into senior programming or data management positions.

What are popular job titles related to Clinical Database Programmer jobs in Michigan? For Clinical Database Programmer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Clinical Database Programmer jobs in Michigan look for? The top searched job categories for Clinical Database Programmer jobs in Michigan are:
What are popular job titles related to Clinical Database Programmer jobs in MI? For Clinical Database Programmer jobs in MI, the most frequently searched job titles are:
Clinical Database Programmer jobs near you
Infographic showing various Clinical Database Programmer job openings in Michigan as of July 2026, with employment types broken down into 86% Full Time, 7% Part Time, 5% Contract, and 2% Summer. Highlights an 81% In-person, and 19% Remote job distribution, with an average salary of $103,687 per year, or $49.8 per hour.
Senior Statistical Programmer - Remote

Senior Statistical Programmer - Remote

MMS

Canton, MI • On-site

Full-time

Posted 24 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

View All M. M. S. Jobs