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Clinical Data Programmer Jobs in Virginia (NOW HIRING)

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: Develop SAS programs for tables, listings, and ...

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: โ€ข Develop SAS programs for tables, listings ...

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements: Key Responsibilities: โ€ข Develop SAS programs for tables, listings ...

Sr Health Interoperability Engineer

Leesburg, VA ยท On-site

$68 - $91/hr

Data Modeling: FHIR US Core & OMOP * Model source health datasets - claims, clinical, and ... Partner with the Sr. Data Engineer and Sr. Solutions Architect to embed interoperability and data ...

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As a Healthcare IT Data Engineer, you will play a pivotal role in designing, developing, and ... Collaborate with cross-functional teams, including data scientists, analysts, clinicians, and IT ...

This role will collaborate with data engineers, analysts, clinicians, and program stakeholders to transform complex healthcare data into actionable insights that improve operations, outcomes, and ...

This role will collaborate with data engineers, analysts, clinicians, and program stakeholders to transform complex healthcare data into actionable insights that improve operations, outcomes, and ...

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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.
Executive Director, Clinical Data Science

Executive Director, Clinical Data Science

Eisai

Charlottesville, VA โ€ข On-site

Full-time

Posted 16 days ago


Job description

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

We are seeking a visionary leader to shape and drive Clinical Data Science strategy across our global clinical development portfolio. This role ensures the rigorous application of statistical principles and advanced data science methodologies to optimize clinical trial efficiency and accelerate innovation. The Executive Director will spearhead the integration of AI/ML solutions for applications in disease diagnosis, modeling, imaging, genomics, proteomics, and precision medicine. Acting as the primary data science representative to global regulatory authorities, this individual will defend strategies and influence industry standards.

Strategic Leadership:

  • Define and execute Clinical Data Science strategies for clinical studies and development plans across the portfolio.
  • Serve as the primary spokesperson for Data Science at Health Authority meetings, leading preparation of responses and influencing regulatory perspectives.

Innovation & Execution:

  • Drive adoption of cutting-edge AI/ML methodologies for disease modeling, biomarker analysis, and precision medicine.
  • Oversee multiple large-scale, critical data science initiatives, ensuring timely, high-quality deliverables aligned with industry best practices.

Risk Management & Problem Solving:

  • Evaluate analytical options, proactively identify risks, and develop novel solutions to complex challenges.

Thought Leadership & External Engagement:

  • Represent the organization at technical seminars and conferences; build networks with industry experts to advance best practices.

Team Leadership & Development:

  • Manage and mentor a diverse team of data scientists and people managers across geographies.
  • Foster career growth through open dialogue, performance management, and strategic development planning.

Operational Excellence:

  • Ensure GxP compliance in data science programming for clinical trials.
  • Manage budgets, vendor relationships, and third-party deliverables to maintain quality and efficiency.

Executive Communication:

  • Deliver clear, compelling communication of complex data science concepts to internal and external stakeholders with executive presence.

Qualifications

  • Ph.D. in Biostatistics or a Master's Degree in Biostatistics in combination with a Ph.D.in Bioinformatics or related computational sciences.
  • Deep expertise in statistical methods and their application in clinical trials.
  • Minimum 10 years of industry experience in clinical development, including Data Science and Biostatistics.
  • Recognized thought leader in at least one data science discipline (e.g., AI/ML modeling, precision medicine).
  • Proven experience presenting at external forums and influencing regulatory authorities.
  • Strong people leadership experience in a Data Science setting.
  • Prior research experience in neurology, particularly Alzheimer's disease biomarkers (plasma, CSF, imaging), strongly preferred.

Eisai Salary Transparency Language:

The annual base salary range for the Executive Director, Clinical Data Science is from :$273,200-$358,600Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

Right To Work

E-Verify Participation


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About Eisai

Sourced by ZipRecruiter

Eisai is a global pharmaceutical company (headquartered in Woodcliff Lake, NJ, US), renowned for its innovative research and development in neuroscience and oncology. The primary focus of the company is to provide therapeutic treatments and solutions for diseases like Alzheimer's, cancer, and other neurological disorders. Eisai was founded in Japan in 1941 and has since developed a strong presence across international markets. Eisai's core values center around their philosophy of 'human health care' (hhc), where they aim to make significant and positive contributions to patients and their families' healthcare worldwide.

Company size

1,001 - 5,000 Employees

Headquarters location

Nutley, NJ, US

Year founded

1995

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