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Remote Statistical Programmer Jobs in Arlington, VA

VENESCO, LLC

SAS Programmer

Falls Church, VA · On-site +1

Remote/Hybrid Job Type: Full-Time Position Overview: Venesco is seeking a skilled SAS Programmer to ... Bachelor's or Master's degree in Statistics or related field 5+ years of SAS programming experience ...

Econometrica

Senior SAS/Python Programmer

Bethesda, MD · On-site +1

... Primary) Remote (Virtual) - US - US Travel About Econometrica, Inc. Econometrica, Inc., is a ... The candidate will work alongside a multidisciplinary team of statistical programmers, data ...

micro1 AI

Director of Biostatistics

Washington, DC · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Alexandria, VA · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Maximus

Data Scientist (Remote)

VA · On-site +1

General information Job Posting Title Data Scientist (Remote) Date Tuesday, August 4, 2026 City ... Statistics, Engineering, Business Administration or a related field preferred. - 1-3+ years of ...

Maximus

Data Scientist II (Remote)

VA · On-site +1

General information Job Posting Title Data Scientist II (Remote) Date Tuesday, August 4, 2026 City ... used statistical software and programming tools, such as SPSS, SAS, Python, and R Shiny ...

ASSYST, Inc.

Software Developer

Sterling, VA · Remote

... statistical analysis, and data science. * Prepare comprehensive test plans, conduct tests, and ... Remote work is not permitted. ASSYST Benefits: We are proud to offer a robust benefits package ...

ASSYST, Inc.

Software Developer

Sterling, VA · Remote

... statistical analysis, and data science. * Prepare comprehensive test plans, conduct tests, and ... Remote work is not permitted. ASSYST Benefits: We are proud to offer a robust benefits package ...

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All JobsStatistical Programmer JobsRemote Statistical Programmer JobsRemote Statistical Programmer Jobs in Arlington, VA

Remote Statistical Programmer information

See Arlington, VA salary details

$97.2K

$169.4K

$286.3K

How much do remote statistical programmer jobs pay per year?

As of Sep 9, 2026, the average yearly pay for remote statistical programmer in Arlington, VA is $169,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $143,700.00 and $184,000.00 per year, depending on experience, location, and employer.

What is a remote statistical programmer?

A remote statistical programmer is a professional who uses statistical software and programming languages to analyze data, typically for research, clinical trials, or business insights, while working from a location outside of a traditional office environment. They are responsible for managing, cleaning, and organizing large datasets, and for developing programs that generate statistical analyses and reports. Remote statistical programmers often collaborate with statisticians, data scientists, and project teams using online communication tools. This role requires strong skills in programming languages such as SAS, R, or Python, and attention to detail when handling complex data. Working remotely provides flexibility but also requires good time management and communication skills.

What does a remote statistical programmer do?

As a remote statistical programmer, you use programming techniques to produce useful data sets from raw data. In this role, you may evaluate the programming needs of each project, use validation techniques to ensure the accuracy of all data sets your programs make, and manage both a database and the operating environment of your software. Remote statistical programmers often work from home and collaborate with other programmers through video calls, voice chat, or remote office software. This job is also known as SAS, which stands for statistical analysis system programming, and companies may advertise under either title.

What are the key skills and qualifications needed to thrive as a remote statistical programmer, and why are they important?

To thrive as a Remote Statistical Programmer, you need strong proficiency in statistics, data analysis, and programming languages like SAS or R, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with statistical software, clinical trial data standards (such as CDISC), and regulatory submission requirements is often necessary. Attention to detail, problem-solving ability, and effective remote communication are essential soft skills for collaborating with cross-functional teams. These competencies ensure high-quality data analysis, regulatory compliance, and seamless teamwork in a remote environment.

How do remote statistical programmers typically collaborate with cross-functional teams despite working remotely?

Remote Statistical Programmers often work closely with biostatisticians, data managers, and clinical research associates using collaborative tools such as video conferencing, project management platforms, and secure data-sharing systems. Regular virtual meetings are scheduled to discuss project progress, address data or programming issues, and align on analysis plans. Clear documentation and version control are essential to ensure seamless teamwork and maintain data integrity. Effective communication skills and proactive updates help bridge the physical distance and contribute to successful project outcomes.

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

AspectRemote Statistical ProgrammerClinical Data Analyst
Required CredentialsBachelor's/Master's in Biostatistics, Statistics, or related field; programming skills in SAS, R, or PythonBachelor's/Master's in Statistics, Data Science, or related; strong analytical and statistical skills
Work EnvironmentRemote or office-based, collaborating with biostatistics teams in clinical trialsRemote or on-site, analyzing clinical data to support study outcomes
Employer & Industry UsagePharmaceuticals, biotech, CROs, clinical research organizationsPharmaceuticals, healthcare, research institutions, CROs

Remote Statistical Programmers focus on programming and data management for clinical trials, while Clinical Data Analysts interpret and analyze clinical data. Both roles require strong statistical skills and often work in similar environments within the healthcare and pharmaceutical industries, but their core responsibilities differ.

More about Remote Statistical Programmer jobs

What are the most commonly searched types of Statistical Programmer jobs in Arlington, VA?

The most popular types of Statistical Programmer jobs in Arlington, VA are:

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For Remote Statistical Programmer jobs in Arlington, VA, the most frequently searched job titles are:

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The top searched job categories for Remote Statistical Programmer jobs in Arlington, VA are:

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Cities near Arlington, VA with the most Remote Statistical Programmer job openings:

Remote Statistical Programmer jobs near you
Infographic showing various Remote Statistical Programmer job openings in Arlington, VA as of August 2026, with employment types broken down into 55% Full Time, and 45% Part Time. Highlights an 100% Remote job distribution, with an average salary of $169,453 per year, or $81.5 per hour.

Principal Biostatistician

Triangle, VA • On-site, Remote

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees
Learn more about Worldwide Clinical Trialsexternal

Full-time

Posted 8 days ago

Job description

Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What The Principal Scientist, Biostatistician does at Worldwide
Use independent judgment and technical expertise to assist in designing studies; preparing statistical analysis plans; analyzing data from pharmacokinetic, clinical, and pre-clinical studies; interpreting statistical results from pharmacokinetic, clinical, and related analyses; and generating randomization schedules for clinical studies.
Principal Scientists are recognized as scientific leaders in the company. They regularly contribute to literature and to building Worldwide Clinical Trials' intellectual property and are capable of leading interdisciplinary project teams.
What you will do
  • Accurately and efficiently perform tasks that are broad in scope

  • Use knowledge and judgment to reach well-defined goals in project management

  • Work independently and collaboratively to solve technical problems by implementing contemporary methods

  • Assist the clinic, method development, and marketing/business development by applying knowledge, conducting literature reviews, providing information, and offering related support

  • Train and guide less experienced personnel in techniques required for work assignments

  • Supervise personnel involved in statistical and pharmacokinetic-related work

  • Assist with the design of clinical studies and construct data analysis plans to meet study protocol requirements and maximize information from available data

  • Perform statistical analyses on clinical and pharmacokinetic data using appropriate methods and software programs

  • Prepare documentation for final reports, including text, tables, graphs, and analysis outputs

  • Interact with clients, bioanalytical personnel, and clinical personnel regarding study design, statistical analyses, pharmacokinetic data analyses, and data interpretation

  • Identify problems or potential problems in generating quality statistical and pharmacokinetic documents, report concerns to their supervisor, and propose possible solutions
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

What your bring to the role
  • Familiarity with corporate policies, goals, and objectives, normally acquired after three months of exposure to Worldwide Clinical Trials' operations

  • Understands and applies Good Laboratory Practice (GLP) guidelines and U.S. Food and Drug Administration (FDA) guidance documents pertinent to statistical analysis, pharmacokinetic studies, pharmacokinetic analyses, and reports

  • Excellent SAS programming skills

  • Proficient in the use of WinNonlin, nQuery, Microsoft Word, and Microsoft Excel

  • Ability to read, write, and understand complex literature

  • Ability to write concise, understandable study reports and communicate clearly with clients and Worldwide Clinical Trials personnel

  • Ability to create, understand, and interpret graphs, tables, and charts

  • Strong organizational and problem-solving skills and ability to set priorities

  • Ability to interact effectively with superiors, peers, and others and communicate ideas clearly

  • Ability to follow and implement Worldwide Clinical Trials' policies and Standard Operating Procedures, normally associated with three months of experience at Worldwide Clinical Trials

Your experience
  • PhD or postgraduate degree with a scientific focus preferred

  • Bachelor's degree with a scientific focus and 12 or more years of relevant work experience required

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $96,500.00 - $191,500.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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