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Clinical Programmer Jobs in Ohio (NOW HIRING)

Clinical Director

Chardon, OH · On-site

$120 - $160/hr

Provide leadership and oversight of all clinical services and programming. * Supervise, mentor, and support therapists and other clinical team members. * Conduct clinical supervision, case ...

Clinical Director

Chardon, OH · On-site

$90 - $140/hr

Provide leadership and oversight of all clinical services and programming. * Supervise, mentor, and support therapists and other clinical team members. * Conduct clinical supervision, case ...

Clinical Director

Chardon, OH

$68K - $93K/yr

Provide leadership and oversight of all clinical services and programming. * Supervise, mentor, and support therapists and other clinical team members. * Conduct clinical supervision, case ...

Clinical Director

Cincinnati, OH · On-site +1

$76K - $104K/yr

The Clinical Director oversees all clinical programming and collaborates with the Leadership team on administrative functions, including providing clinical services, supervising and evaluating ...

Showing results 21-40

Clinical Programmer information

See Ohio salary details

$23

$61

$97

How much do clinical programmer jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical programmer in Ohio is $61.58, according to ZipRecruiter salary data. Most workers in this role earn between $50.96 and $69.71 per hour, depending on experience, location, and employer.

What is a clinical programmer?

Clinical programmers are professionals who design, develop, and maintain computer programs used to manage and analyze clinical trial data in the pharmaceutical and biotech industries. They work closely with data managers, statisticians, and clinical teams to ensure data accuracy and regulatory compliance. Their responsibilities often include writing programs for data cleaning, statistical analysis, and generating reports using tools like SAS or R. Clinical programmers play a key role in ensuring that clinical trial data is processed efficiently and meets industry standards.

What are the key skills and qualifications needed to thrive as a clinical programmer?

To thrive as a Clinical Programmer, you need strong proficiency in programming languages like SAS or R, a solid understanding of clinical trial processes, and typically a degree in life sciences, computer science, or a related field. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and CDISC standards such as SDTM and ADaM is often required. Attention to detail, problem-solving ability, and effective communication are vital soft skills for ensuring data accuracy and collaborating with cross-functional teams. Mastery of these skills ensures the integrity and reliability of clinical trial data, supporting regulatory compliance and successful study outcomes.

How does a clinical programmer typically collaborate with biostatisticians and data managers during a clinical trial?

Clinical Programmers work closely with biostatisticians and data managers throughout the clinical trial process. They are responsible for programming data listings, tables, and figures based on statistical analysis plans provided by biostatisticians. Collaboration involves ensuring data integrity, resolving data discrepancies, and implementing database validation checks, often through regular meetings and shared documentation. This teamwork is essential for maintaining data quality and meeting regulatory requirements, making strong communication and coordination skills important in the role.

What is the difference between Clinical Programmer vs Data Manager?

AspectClinical ProgrammerData Manager
Required CredentialsBachelor's degree in life sciences, computer science, or related field; programming skills in SAS, R, or SQLBachelor's degree in health sciences, statistics, or related field; experience with data management software
Work EnvironmentCollaborates with statisticians, data managers, and clinical teams to develop and validate data reportsOversees data collection, validation, and database management for clinical trials
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

While both Clinical Programmers and Data Managers work within clinical research, Clinical Programmers primarily focus on developing data reports and programming analysis datasets, whereas Data Managers handle data collection, validation, and database management. Both roles require strong analytical skills and familiarity with clinical data standards, often working closely together to ensure data quality and integrity in clinical trials.

Infographic showing various Clinical Programmer job openings in Ohio as of August 2026, with employment types broken down into 2% As Needed, 71% Full Time, 18% Part Time, and 9% Contract. Highlights an 82% Physical, 1% Hybrid, and 17% Remote job distribution, with an average salary of $128,088 per year, or $61.6 per hour.

Clinical Database Programmer-Reference Laboratory

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

16th of 75 rated research


Job description

Job Summary
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team. This position will work in a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
  • Communicate with internal teams at Medpace Reference Laboratories (MRL) regarding study progress;
  • Work closely with the Project Management team to setup, validate, and maintain study databases according to sponsor specifications; and
  • Programming responsibilities entail using syntax built specifically for MRL to build custom expressions that meet specific sponsor requests.
  • Act as the primary data management contact for ongoing projects, which includes:
    • Supplying technical support to internal Medpace personnel;
    • Ensuring quality of the database build; and
    • Following up on the progress of projects to ensure sponsor timeline expectations are met.

Qualifications
  • A minimum of a bachelor's degree is required (preferably in a math, science, or informatics related field).
    • Training related to the database build/programming responsibilities is provided once hired for the positions, therefore no prior programming experience is required.
  • Ability to prioritize and manage multiple projects simultaneously;
  • Excellent verbal and written communication skills;
  • Proficient at working in a team environment;
  • Strong attention to detail and accuracy; and
  • Data entry and data management experience is a plus.

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience
    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992