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Remote Pharmaceutical Sas Programmer Jobs (NOW HIRING)

DLH

Research Analyst (SAS and R) (Job 1368)

$50K - $70K/yr

This position is 100% remote . However, employees may be required to attend occasional in-person ... set, SAS programming, and output files. * Conduct geospatial and molecular HIV analysis and ...

Slipstream IT

Statistical Analytical Programmer

PA · On-site +1

This person will bring strong SAS programming experience and a practical understanding of ... Able to work independently in a remote environment and manage timelines effectively. Preferred ...

Slipstream IT

Statistical Analytical Programmer

PA · Remote

This person will bring strong SAS programming experience and a practical understanding of ... Able to work independently in a remote environment and manage timelines effectively. Preferred ...

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

Performs quality control checks of SAS code and output produced by other Statistical Programmers to ... S. years of work experience in Biotech, Pharmaceuticals or Clinical Research Organization Pay Range ...

Kraken Robotics

Software Developer Level 2, SAS

This position could be Remote, US or in one of our US Offices. The Software Developer Level II, SAS will work on our real-time SAS platform. This is a high-impact role: as a Software Developer Level ...

Gilead Sciences, Inc.

Statistical Programmer II

$107K - $138K/yr

Uses internal macros or writes SAS ® macros to automate study deliverables. * Assists in ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.

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How much do remote pharmaceutical sas programmer jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for remote pharmaceutical sas programmer in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

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

AspectRemote Pharmaceutical Sas ProgrammerRemote Clinical Data Analyst
Required CredentialsBS in Computer Science, Life Sciences, or related field; SAS certification often preferredBSc in Life Sciences, Statistics, or related; often requires knowledge of data management tools
Work EnvironmentPharmaceutical companies, CROs, or biotech firms; primarily remote or hybridResearch organizations, CROs, pharmaceutical companies; mostly remote
Employer & Industry UsageUsed in clinical trial data programming, reporting, and analysisUsed in data cleaning, management, and statistical analysis of clinical data

The Remote Pharmaceutical Sas Programmer focuses on developing and validating SAS programs for clinical trial data, while the Remote Clinical Data Analyst emphasizes analyzing and managing clinical data sets. Both roles require familiarity with clinical research processes and often share similar certifications, but their core responsibilities differ in programming versus data analysis tasks.

What are the key skills and qualifications needed to thrive as a Remote Pharmaceutical SAS Programmer, and why are they important?

To thrive as a Remote Pharmaceutical SAS Programmer, you need strong expertise in statistical programming, clinical trial data analysis, and a solid understanding of regulatory requirements, typically supported by a degree in statistics, computer science, or a related field. Proficiency with SAS software (Base, Macro, STAT) and familiarity with CDISC standards (SDTM, ADaM) and FDA submission processes are crucial. Exceptional attention to detail, problem-solving skills, and effective communication are vital soft skills for collaborating with global teams and ensuring data integrity. These skills and qualifications are essential to produce accurate, compliant datasets and reports that support successful drug development and regulatory approval.

What is a Remote Pharmaceutical SAS Programmer?

A Remote Pharmaceutical SAS Programmer is a professional who uses the SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data for pharmaceutical companies, while working remotely. They transform raw clinical data into meaningful statistical outputs, including tables, listings, and figures required for regulatory submissions. Typically, they collaborate with biostatisticians, clinical data managers, and other team members to ensure data integrity and compliance with industry standards. This role requires strong programming skills, attention to detail, and familiarity with clinical trial processes.

How does a Remote Pharmaceutical SAS Programmer typically collaborate with cross-functional teams during clinical trials?

Remote Pharmaceutical SAS Programmers frequently work with clinical data managers, statisticians, and project managers to ensure accurate data analysis and reporting during clinical trials. Collaboration often happens through virtual meetings, shared documentation, and project management tools, requiring strong communication and organizational skills. Programmers are responsible for translating statistical analysis plans into validated SAS code, performing data cleaning, and generating tables, listings, and figures. Consistent communication and proactive status updates help ensure that project timelines are met and regulatory requirements are adhered to, even while working remotely.
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Remote Pharmaceutical Sas Programmer jobs near you
Infographic showing various Remote Pharmaceutical Sas Programmer job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 40% Full Time, and 55% Part Time. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

Senior Statistical Programmer (Remote)

Everest Clinical Research

Remote

$90K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

Job description

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham Ontario, Canada with additional locations in: Bridgewater, New Jersey; Shanghai, China; Taipei, Taiwan; and multiple offices in Europe.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us...that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities
  • Design and specify study data tabulation models and analysis data models for clinical trials or for the integration of clinical trial data from multiple trials (e.g. ISS and ISE datasets). These designs and specifications are completed in accordance with common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor's requirements.
  • Generate complete and efficient analysis data models following approved dataset designs or specifications. Perform independent validation of datasets created by other programmers or statisticians.
  • Develop SAS programming codes and generate complete and accurate statistical output reports of trial data in well-defined formats.
  • Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers or statisticians.
  • Develop and test SAS codes for clinical trial database logical checks and reports for ongoing data review.
  • Document data and programming information in accordance with corporate SOPs and guidelines.
  • Archive clinical trial data (study data tabulation models and analysis data models) and programming information in accordance with corporate archival SOPs and guidelines.
  • Develop and provide expertise in other programming and system administration areas when required.
  • Provide technical guidance and support to less experienced Statistical Programmers.
  • Contribute to the continuous improvement of the statistical programming processes and procedures.
  • Contribute to the establishment of therapeutic area programming standards/conventions/procedures within assigned therapeutic areas as a lead programmer.
  • Contribute to the establishment of client specific programming standards/conventions/procedures for assigned clients when required.

Qualifications And Experience
  • A Master's in Math/Statistics with at least five years experience

Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $90,000 - $140,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#INDHP
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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