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Clinical R Programmer Jobs in Washington, DC (NOW HIRING)

GLOTECH, Inc

Biostatisticians

Rockville, MD · On-site

... clinical trials, and epidemiological studies that explore health processes; examines the impact of ... Develops code in SAS, R, MPlus, SPSS & Stata * Provides analytic programming support for all phases ...

GLOTECH, Inc

Biostatisticians

Rockville, MD · On-site

... clinical trials, and epidemiological studies that explore health processes; examines the impact of ... Develops code in SAS, R, MPlus, SPSS & Stata * Provides analytic programming support for all phases ...

Ripple Effect

NLM Software Developer

Rockville, MD

$98K - $113K/yr

Work closely with interdisciplinary teams of researchers, data scientists, clinicians, and IT ... Proficiency in programming languages such as C++, Python, Java, JavaScript, R, and scripting ...

Ripple Effect

NLM Software Developer

Rockville, MD · On-site

$98K - $113K/yr

Work closely with interdisciplinary teams of researchers, data scientists, clinicians, and IT ... Proficiency in programming languages such as C++, Python, Java, JavaScript, R, and scripting ...

Ripple Effect

NLM Software Developer

Rockville, MD · On-site

$98K - $113K/yr

Work closely with interdisciplinary teams of researchers, data scientists, clinicians, and IT ... Proficiency in programming languages such as C++, Python, Java, JavaScript, R, and scripting ...

Ripple Effect

NLM Sr. Software Developer

Rockville, MD · On-site

$118K - $135K/yr

Work closely with interdisciplinary teams of researchers, data scientists, clinicians, and IT ... Proficiency in programming languages such as C++, Python, Java, JavaScript, R, and scripting ...

Ripple Effect

NLM Sr. Software Developer

Rockville, MD · On-site

$118K - $135K/yr

Work closely with interdisciplinary teams of researchers, data scientists, clinicians, and IT ... Proficiency in programming languages such as C++, Python, Java, JavaScript, R, and scripting ...

Ripple Effect

NLM Sr. Software Developer

Rockville, MD

$118K - $135K/yr

Work closely with interdisciplinary teams of researchers, data scientists, clinicians, and IT ... Proficiency in programming languages such as C++, Python, Java, JavaScript, R, and scripting ...

Tempus

Director, Biostatistics

Triangle, VA · On-site

$190K - $260K/yr

... Programmers, Clinical Operations, Data Managers, etc. * Thorough understanding of statistical principles and clinical experiment methodology. * Computational skills using R, and/or SAS, especially ...

Gritter Francona

Lead Data Scientist

Washington, DC · On-site

Programming languages (e.g., Python, R) and frameworks (e.g., TensorFlow, PyTorch); Data visualization tools (e.g., Power BI, Tableau) and ETL processes; * Proven experience integrating clinical ...

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All JobsClinical R Programmer JobsClinical R Programmer Jobs in Washington, DC

Clinical R Programmer information

See Washington, DC salary details

$28

$73

$116

How much do clinical r programmer jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical r programmer in Washington, DC is $73.36, according to ZipRecruiter salary data. Most workers in this role earn between $60.72 and $83.03 per hour, depending on experience, location, and employer.

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

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 Clinical R Programmers?

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 are some 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, DC? For Clinical R Programmer jobs in Washington, DC, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Washington, DC look for? The top searched job categories for Clinical R Programmer jobs in Washington, DC are:
Clinical R Programmer jobs near you
Medical Director, Respiratory, Early Clinical Development

Medical Director, Respiratory, Early Clinical Development

AstraZeneca

Gaithersburg, MD • On-site

$249K - $374K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

18th of 74 rated pharmaceutical

Job description

Are you ready to shape and deliver the AstraZeneca Respiratory pipeline?
If you are a motivated drug developer, this is an excellent time to join!
Who We Are
In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers of key respiratory diseases, with access to pioneering science, innovative drug discovery approaches and key collaborations with academic centers around the world. We are investigating a wide range of drug modalities - small molecules, biologics, oligonucleotides and other modalities - across multiple diseases with high unmet medical need.
TSCD in Respiratory is where science meets clinical drug development with a focus upon delivering innovative, early phase clinical studies (Phase 1 - Phase 2), while collaborating closely with our late phase clinical development colleagues who guide later phase clinical studies. We are a diverse team of experienced physicians, clinical scientists and translational medicine scientists who collaborate with scientists and late clinical development to define our early phase clinical development strategies, design innovative clinical trials, develop and validate new clinical endpoints and translate scientific ideas to proof-of-concept studies in targeted patient populations.
What You Will Do
Asa Medical Director, you will provide medical and scientific input to preclinical and clinical stage assets within the context of a respiratory clinical team. This will include the creation of overall clinical development plans and clinical study design as well writing protocols, key study and health authority documentation, medical monitoring and ensuring timely delivery of studies, all in close collaboration with internal and external partners and clinical research organizations.
Experience in Respiratory Medicine is strongly preferred. The successful candidate will thrive in a fast-paced, proactive can-do culture, be a strong communicator, and a collaborator.
  • Responsible for the design, delivery and interpretation of clinical studies ensuring the ethical and scientific integrity of the plans, studies and product in compliance with GCP.

  • Provide guidance in the medical strategy and clinical/disease expertise to Research, Translational Medicine, Early and Late-stage Clinical Development and Commercial colleagues as part of across functional teams.

  • Closely follow medical developments within respiratory diseases and disseminate new information within Clinical Development and the wider organization to transform trends and emerging data into agile and innovative clinical plans.

  • Work closely and collaborate across early and late R&I clinical development, partner functions and wider AZ organization to ensure design and delivery of clinical development plans with high quality and speed.

  • Represent Early Respiratory TSCD to external partners, including Investigators, key external experts and patient advocacy groups.

  • Medical Lead for regulatory communication and preparation of higher level documents

  • Ensures internal and external peer review of potential study/program design.

  • Support qualification of pharmacodynamic/disease markers for early assessment of efficacy.

  • Support establishing scientific collaborations with academic collaborators to support key advancing translational science activities

  • As available, provide clinical strategic input to in-licensing opportunities.

Basic Qualifications:
  • MD or PhD in respiratory sciences or related field

  • Minimum of 5 years experience in industry or relevant clinical or research experience.

  • Understanding of the drug development process, including clinical and non-clinical study design and execution.

  • Understanding of clinical research methodology and biostatistics principles to facilitate innovative and efficient clinical trial design, and clinical development plans with clear data-driven decision rules.

  • Understanding of FDA, MHRA and ICH GCP guidelines to ensure the appropriate conduct of global clinical studies in the United States, Europe, and the rest of the world.

  • Attention to detail, internal drive to generate high-quality work, and sense of passion and urgency to achieve team and program goals.

  • Demonstrated experience managing complex projects and working collaboratively with multiple stakeholders regarding new strategies to ensure consistent communication.

  • Demonstrated track record in delivering results.

  • Outstanding verbal and written communication skills.

  • Excellent analytical, problem solving and strategic planning skills.

The annual base salary for this position ranges from $249,827 - $374,740. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program. Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
Join us in our unique and ambitious world.
Date Posted
07-May-2026
Closing Date
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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