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Clinical Data Programmer Jobs in Virginia (NOW HIRING)

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Collaborate with cross-functional teams, including data scientists, analysts, clinicians, and IT ... Familiarity with at least one programming language such as Python, Java, or C# * Ability to ...

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 ...

Epic Clarity Report Senior Consultant

Mclean, VA · Hybrid

$106K - $129K/yr

Active Certification in Cogito, Clarity Data Model, Caboodle Data Model, Clinical Data model ... These solutions are powered by engineering for business advantage, transforming mission-critical ...

Epic Clarity Report Senior Consultant

Rosslyn, VA · Hybrid

$119K - $145K/yr

Active Certification in Cogito, Clarity Data Model, Caboodle Data Model, Clinical Data model ... These solutions are powered by engineering for business advantage, transforming mission-critical ...

Epic Clarity Report Senior Consultant

Richmond, VA · Hybrid

$103K - $126K/yr

Active Certification in Cogito, Clarity Data Model, Caboodle Data Model, Clinical Data model ... These solutions are powered by engineering for business advantage, transforming mission-critical ...

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Showing results 1-20

Clinical Data Programmer information

See Virginia salary details

$68.9K

$117.9K

$210.2K

How much do clinical data programmer jobs pay per year?

As of Jun 16, 2026, the average yearly pay for clinical data programmer in Virginia is $117,942.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,300.00 and $178,500.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Data Programmer vs Clinical Data Analyst?

AspectClinical Data ProgrammerClinical Data Analyst
Required CredentialsBachelor's in Life Sciences, Biostatistics, or related field; knowledge of programming languages like SAS or RBachelor's in Statistics, Data Science, or related; strong analytical skills
Work EnvironmentClinical trial data management teams, often in CROs or pharmaceutical companiesData analysis teams, often in healthcare or research organizations
Employer & Industry UsageUsed in clinical research to prepare datasets for analysisUsed to interpret data, generate reports, and support decision-making

While both roles involve working with clinical data, Clinical Data Programmers focus on coding and preparing datasets, whereas Clinical Data Analysts interpret data and generate insights. Understanding these differences helps in choosing the right career path or job search focus.

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

To thrive as a Clinical Data Programmer, you need a strong background in programming (especially SAS or SQL), understanding of clinical trial data, and a degree in life sciences, statistics, or a related field. Familiarity with electronic data capture systems, CDISC standards (SDTM/ADaM), and regulatory requirements is typically expected, and relevant certifications can be advantageous. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring data integrity and collaborating with cross-functional teams. These skills and qualifications are vital for producing accurate, regulatory-compliant datasets that support clinical research and successful drug development.

What are Clinical Data Programmers?

Clinical Data Programmers are professionals who manage, process, and analyze clinical trial data using specialized programming languages and software. They are responsible for creating and validating programs that ensure data collected during clinical studies is accurate, consistent, and ready for statistical analysis. Their work is essential to the integrity of clinical research, enabling regulatory submissions and supporting medical decision-making. Clinical Data Programmers often work closely with clinical data managers, statisticians, and other clinical research professionals.

How does a Clinical Data Programmer typically collaborate with clinical research teams during a study?

Clinical Data Programmers work closely with clinical research associates, data managers, biostatisticians, and project managers to ensure the integrity and accuracy of clinical trial data. They often participate in study setup meetings, provide input on case report form (CRF) design, and develop programs for data validation and cleaning. Regular communication is essential to resolve any discrepancies or issues that arise during data collection and to implement mid-study changes. This collaborative environment ensures that the data is reliable and meets regulatory requirements.
What are popular job titles related to Clinical Data Programmer jobs in Virginia? For Clinical Data Programmer jobs in Virginia, the most frequently searched job titles are:
Infographic showing various Clinical Data Programmer job openings in Virginia as of June 2026, with employment types broken down into 2% As Needed, 92% Full Time, and 6% Part Time. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $117,942 per year, or $56.7 per hour.
2025 Fall Intern, Clinical Applications

2025 Fall Intern, Clinical Applications

Zimmer Biomet

Chesapeake, VA

$13 - $17.50/hr

Other

Posted 24 days ago


Zimmer Biomet rating

7.8

Company rating: 7.8 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

173rd of 418 rated machine equipment manufacturers


Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.  

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.  We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of software used in clinical research, primarily the Clinical Trial Management System (CTMS). 

How You'll Create Impact
  • Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts.
  • Support the documentation of technical processes, user guides, and validation protocols.
  • Participate in requirements gathering sessions with stakeholders to better understand business and user needs.
  • Help monitor and track system issues, assisting in troubleshooting with supervision.
  • Perform basic data checks and assist with data validation efforts to ensure data integrity.
  • Observe and support user training sessions and help prepare training materials as needed.
What Makes You Stand Out
  • Strong written and verbal communication skills.
  • Ability to manage time effectively and handle multiple tasks or assignments under supervision.
  • Ability to work collaboratively as part of a team and communicate effectively with both technical and non-technical stakeholders.
  • Detail-oriented mindset with the ability to follow documented procedures and best practices.
  • Curiosity and willingness to learn about clinical applications and how technology supports clinical trials and research.
  • Proficiency in Microsoft Office tools, especially Excel, Word, and PowerPoint.
  • Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or similar.
  • Basic understanding of relational databases and familiarity with writing or reading simple SQL queries is a plus.
  • Interest in web development and knowledge of HTML and CSS, or UX/UI is a plus.
Your Background
  • Must be actively enrolled in an academic program for the entire duration of the assignment
  • Must be available to work full-time (40 hours/week) throughout the co-op session
  • Must be authorized to work in the U.S. without requiring employer sponsorship
  • Pursuing a bachelor’s degree in Computer Science, Information Systems, Health Informatics, Data Science, or related field.
  • A minimum GPA of 3.0 is strongly preferred
Travel Expectations
  • Up to 5%

EOE/M/F/Vet/Disability


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About Zimmer Biomet

Sourced by ZipRecruiter

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Warsaw, IN, US

Year founded

1927

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