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Statistical Programmer Jobs in Indiana (NOW HIRING)

CMM Programmer Job Summary: The CMM Programmer is responsible for developing and executing ... providing statistical reports reflecting process control, process capability and gauge ...

Quality Engineer

Bluffton, IN · On-site

$65K - $84K/yr

The Quality Engineer ensures that products being built and processes being used adhere to all ... Analyzes statistical data and product specifications to determine standards and establish quality ...

Quality Engineer

Bluffton, IN · On-site

$65K - $84K/yr

The Quality Engineer ensures that products being built and processes being used adhere to all ... Analyzes statistical data and product specifications to determine standards and establish quality ...

Bachelor's or master's degree in data science, Computer Science, Statistics, Engineering, or a related field. * 4+ years of experience in data science or advanced analytics. * Hands-on experience ...

Manufacturing Engineer

Evansville, IN · On-site

$69K - $88K/yr

The Manufacturing Engineer will work cross-functionally with Production, Maintenance, Quality, and ... Utilize statistical tools (SPC, capability analysis, DOE, root cause analysis) to identify and ...

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

Job Title Quality Engineer About your role: Join our Output Solutions team within Fiserv as a ... You will serve as a change leader, applying advanced statistical methods, Lean and Six Sigma ...

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

Job Title Quality Engineer About your role: Join our Output Solutions team within Fiserv as a ... You will serve as a change leader, applying advanced statistical methods, Lean and Six Sigma ...

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Showing results 1-20

Statistical Programmer information

See Indiana salary details

$80.4K

$140.2K

$236.9K

How much do statistical programmer jobs pay per year?

As of Jun 4, 2026, the average yearly pay for statistical programmer in Indiana is $140,157.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,900.00 and $152,200.00 per year, depending on experience, location, and employer.

What Does a Statistical Programmer Do?

A statistical programmer creates statistical programming deliverables. You ensure excellent programming of analysis-ready data, tables, and figures. You may use Stata for general purpose statistical analysis or SPSS for interactive or batched statistical analysis. Your responsibilities include developing standard operating procedures and complying with guidelines. Other duties include remaining informed on developments in programming standards and meeting all regulatory requirements. You also create PROC statements that call upon named procedures for analysis. You develop programs for dataset integration, prepare resource plans, and assist with quality control of datasets.

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

To thrive as a Statistical Programmer, you need a strong background in statistics, data analysis, and programming—typically with a degree in statistics, mathematics, computer science, or a related field. Expertise in statistical software such as SAS, R, or Python and familiarity with data management systems like CDISC or SQL are often required, along with relevant certifications. Strong problem-solving abilities, attention to detail, and clear communication skills help you interpret data accurately and collaborate effectively with cross-functional teams. These skills ensure the delivery of high-quality, reproducible statistical analyses crucial for informed decision-making in research and industry settings.

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

Statistical Programmers often encounter challenges such as managing large, complex datasets, ensuring data integrity, and adhering strictly to regulatory standards (like CDISC SDTM and ADaM). They must also collaborate closely with biostatisticians and data managers to accurately translate statistical analysis plans into code. Tight project timelines and shifting priorities can require strong organizational skills and adaptability. Effective communication and attention to detail are essential for navigating these challenges and delivering reliable results.

What are statistical programmers?

Statistical programmers are professionals who use statistical software and programming languages, such as SAS, R, or Python, to manage, analyze, and report data, often in clinical trials, public health, or research settings. They play a crucial role in transforming raw data into meaningful results by writing code for data cleaning, data manipulation, statistical analysis, and generating reports. Statistical programmers often work closely with statisticians, data managers, and researchers to ensure the accuracy and integrity of data analyses. Their work is essential in industries like pharmaceuticals, healthcare, and academia.

Is SAS a good career choice?

A career as a Statistical Programmer using SAS is in demand in industries such as pharmaceuticals, healthcare, and research, where data analysis and reporting are essential. Proficiency in SAS, along with knowledge of programming and statistical methods, can lead to stable employment and opportunities for advancement.

What is the difference between Statistical Programmer vs Data Analyst?

AspectStatistical ProgrammerData Analyst
Required CredentialsBachelor's in Statistics, Biostatistics, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and data managementVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesUsed across multiple sectors like finance, retail, and healthcare

While both roles handle data, Statistical Programmers primarily focus on programming and managing clinical or research data, whereas Data Analysts interpret data to generate insights across various industries. The roles often overlap in skills like statistical software proficiency but differ in their core responsibilities and industry focus.

What are the most commonly searched types of Statistical Programmer jobs in Indiana? The most popular types of Statistical Programmer jobs in Indiana are:
What job categories do people searching Statistical Programmer jobs in Indiana look for? The top searched job categories for Statistical Programmer jobs in Indiana are:
What cities in Indiana are hiring for Statistical Programmer jobs? Cities in Indiana with the most Statistical Programmer job openings:
Infographic showing various Statistical Programmer job openings in Indiana as of May 2026, with employment types broken down into 4% Internship, 92% Full Time, and 4% Contract. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $140,157 per year, or $67.4 per hour.
eCOA - Clinical Study Build Programmer

eCOA - Clinical Study Build Programmer

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 71 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
The Clinical Study Build Programmer - eCOA is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in-depth understanding of data technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager and other key business partners to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.
Portfolio Delivery
  • Proficiency in programming and configuring clinical data collection systems (e.g., eCOA/EDC platforms)
  • Study build programming expertise (e.g., form logic, edit checks, workflows, integrations)
  • Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
  • Gather and influence eCOA design specifications and enable successful implementation
  • Understand study translation needs and enable localization
  • Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives
  • Provide insights into the study design and data delivery (i.e. Data Management Plan, Project Plan, database, and observed datasets)
  • Support submission, inspection and regulatory response activities
  • Lead cross Business Unit/Therapeutic Area projects or programs with high complexity
  • Possess a deep understanding of the technology used to collect clinical trial data
  • Develops and tests new ideas and/or applies innovative solutions

Project Management
  • Increase speed, accuracy, and consistency in the development of systems solutions
  • Enable metrics reporting of study development timelines and pre and post production changes to database
  • Partner with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Management Associate to deliver study database per business need and before first patient visit
  • Influence data standard decisions and strategies for a study and/or program
  • Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study database building
  • Integrates multi-functional, external information and technical knowledge to support data-driven decision making

Enterprise Leadership
  • Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis
  • Work to reduce postproduction changes change control process
  • Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization
  • Thinks with end to end in mind consistently managing risk to minimize impact on delivery
  • Strong awareness with external developments, timelines
  • Focuses on defining database solutions and timelines in support of advancing the portfolio

Minimum Qualification Requirements:
  • Master's degree in a scientific field such as Informatics/Analytics, Life Sciences, Statistics, Information Technology, Epidemiology, Computer Sciences
  • + 3 years of related experience (or bachelor's degree plus 5 or more years of experience in clinical data management or areas that closely intersect with clinical data management e.g., statistics, data analytics, information technology, health outcomes, etc...)

Additional Preferences:
  • Experience with designing and handling eCOA data Articulating the flow of data (structure and format) from patient to analysis, applying this knowledge to data solutions
  • Deciding the technology platform (system/database) for data acquisition and aggregation Utilization of clinical/drug development knowledge and an ability to liaise with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical, etc.)
  • Strong therapeutic/scientific knowledge in the field of research Familiarity with clinical data tools and technologies
  • Understanding and experience in using data standards Ability to balance multiple activities, prioritize and manage ambiguity Domestic and International travel may be required

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$79,500 - $169,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876