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Clinical R Programmer Jobs in Washington (NOW HIRING)

Emmes Group

Senior Biostatistician

Rockville, MD · On-site

... clinical research required. * 1-3 years Strong programming skills in SAS and/or R required. Why work at Emmes? At Emmes, your actions and hard work will have a direct impact on public health ...

Emmes

Senior Biostatistician

Rockville, MD · On-site +1

... clinical research required. * 1-3 years Strong programming skills in SAS and/or R required. Why work at Emmes? At Emmes, your actions and hard work will have a direct impact on public health ...

Emmes

Senior Biostatistician

Rockville, MD · On-site

... clinical research required. * 1-3 years strong programming skills in SAS and/or R required. Why work at Emmes? At Emmes, your actions and hard work will have a direct impact on public health ...

Axle

Data Scientist II

Rockville, MD · On-site

... clinician-researchers, data engineers, software developers, and government stakeholders to ensure ... Strong proficiency in Python and R for analysis, scripting, and visualization. Hands-on experience ...

Phase2 Technology

Health Data Scientist

Washington, DC · On-site

$86K - $198K/yr

Here,you'llwork with and guide a multi-disciplinary team of analysts, data engineers, clinical SMEs ... Experience with R, Scala, or Java * Experience retrieving, parsing, and processing structured and ...

Vhr_unither

Co-op - Computational Lab

Silver Spring, MD · On-site

... affect clinical measurements related to hemodynamics and pulmonary function testing * Apply ... R, Python, Julia, Matlab, or other programming language Eligible employees may participate in the ...

Federallabs

Program Manager - TBICOE

Silver Spring, MD · On-site

TBICoE is a branch of the Research Support Division in the Research and Engineering Directorate (R ... HJF's support and administrative capabilities allow military medical researchers and clinicians to ...

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Clinical R Programmer information

What is a Clinical R programmer?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What skills and qualifications are needed to be a Clinical R programmer?

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are common challenges faced by Clinical R programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Washington?

For Clinical R Programmer jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Clinical R Programmer jobs in Washington look for?

The top searched job categories for Clinical R Programmer jobs in Washington are:

What cities in Washington are hiring for Clinical R Programmer jobs?

Cities in Washington with the most Clinical R Programmer job openings:

Clinical R Programmer jobs near you
Infographic showing various Clinical R Programmer job openings in Washington as of September 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 84% In-person, and 16% Remote job distribution.

Senior Biostatistician

Rockville, MD • On-site

Emmes Group
See more jobs at Emmes Groupexternal

Full-time

Medical, Retirement

Re-posted 23 days ago

Job description

Overview
Senior Biostatistician
US Remote
Emmes Group: Building a better future for us all.
Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.
We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!
Primary Purpose
Leads collaborations with clinical investigators to determine study design, contributes to protocol development, authors statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer reviewed journals. Manages statistical activities for a clinical study or platform of clinical studies.
Responsibilities
  • Provides sound strategic, scientific and statistical input to support client's research projects.
  • Serves as the lead Biostatistician on one or more study projects.
  • May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies.
  • Leads the project team's development of study analysis plans and statistical programs to perform analyses and display study data.
  • Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted.
  • Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.
  • Ensures the scientific integrity of the research project and the accuracy of the reported results.
  • Performs sample size calculation and provides leadership in the statistical design of research projects.
  • Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.
  • Develops study assignment allocation schemas along with appropriate documentation.
  • Leads the development of the methods and results sections of clinical study reports and scientific publications.
  • Represents EMMES on behalf of clients at regulatory meetings.
  • Participate in the development and updating of Standard Operating Procedures.
  • Performs other duties as assigned
  • Complies with all policies and standards

Qualifications
  • PhD or MS in Biostatistics, statistics, epidemiology or related field required
  • 4-6 years of related experience is expected but not required for the position.
  • 1-3 years Demonstrated proficiency with statistical methods and applications in clinical research required.
  • 1-3 years Strong programming skills in SAS and/or R required.

Why work at Emmes?
At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:
  • Flexible Approved Time Off

  • Tuition Reimbursement

  • 401k Retirement Plan
  • Work From Home Anywhere in the US

  • Maternal/Paternal Leave

  • Casual Dress Code & Work Environment

CONNECT WITH US!
Follow us on Twitter - @EmmesCRO
Find us on LinkedIn - Emmes
The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.
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