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Remote Clinical Sas Programmer Jobs (NOW HIRING)

EDETEK

Senior Statistical Programmer

... SAS and R, as well as a deep understanding of clinical trial methodology and regulatory ... This is a remote position, and we are open to candidates based in the United States, Bulgaria ...

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 ...

Calyx

Clinical Data Programmer I

$52K - $75K/yr

Understanding of 21 CFR Part 11 * Entry level SAS programming experience * Experience with EDC (e.g ... Previous experience in data management role This role is remote based. Open to candidates located ...

MM International

Data Scientist

New York, NY · Remote

Remote Duration 4-6 months The RBQM Data Scientist supports central monitoring and risk-based ... using clinical data, with strong emphasis on SAS programming to deliver robust and scalable ...

Adecco

Statistician/Biostatistician

North Chicago, IL · On-site +1

$45/hr

The ideal candidate will have strong SAS programming skills, experience with clinical or analytical ... Remote * Schedule: Monday-Friday, 8:00 AM-5:00 PM * Overtime: Possible based on business needs

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

As of Jul 23, 2026, the average hourly pay for remote clinical sas programmer in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What typical projects and responsibilities can I expect as a Remote Clinical SAS Programmer?

As a Remote Clinical SAS Programmer, you'll primarily support clinical trial data analysis by programming tables, listings, and figures (TLFs), creating datasets, and ensuring data integrity. You will collaborate closely with biostatisticians, data managers, and other clinical team members to provide statistical outputs for clinical study reports and regulatory submissions. Your daily tasks include writing and validating SAS code, documenting work for audit purposes, and adhering to industry standards such as CDISC. The role often involves juggling multiple projects simultaneously, offering variety and opportunities to deepen your expertise in clinical data. This environment is well-suited to self-motivated professionals seeking both autonomy and collaborative teamwork in a dynamic, impactful field.

What Does a Remote SAS Clinical Programmer Do?

The job duties of a remote SAS clinical programmer involve programming within the Statistical Analysis System (SAS) software suite. You perform your responsibilities for this virtual job from a remote location outside of your client or employer’s office. A clinical SAS programmer focuses on clinical data collection and analysis. After gathering the required dataset, you analyze the data using SAS software to find the desired information about healthcare services, clinical trials, or other similar subjects. You then document the results of the analysis.

What is a Remote Clinical SAS Programmer job?

A Remote Clinical SAS Programmer is responsible for programming, validating, and analyzing clinical trial data using SAS software while working from a remote location. They collaborate with biostatisticians and clinical teams to create datasets, generate tables, listings, and figures, and ensure compliance with regulatory standards such as CDISC, SDTM, and ADaM. Their work supports drug development and regulatory submissions, making accuracy and efficiency crucial. Strong SAS programming skills, knowledge of clinical research, and experience with regulatory guidelines are essential for this role.

What are the key skills and qualifications needed to thrive in the Remote Clinical Sas Programmer position, and why are they important?

To thrive as a Remote Clinical SAS Programmer, you need strong statistical analysis skills, proficiency in SAS programming, and a background in clinical trials or life sciences. Experience with CDISC standards, clinical databases, and regulatory compliance, as well as certifications like SAS Certification or knowledge of SDTM and ADaM, are highly valued. Attention to detail, excellent communication, and time management are critical soft skills for remote collaboration and meeting project timelines. These attributes ensure reliable data outputs, successful teamwork, and compliance with industry regulations in a remote clinical research environment.

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What cities are hiring for Remote Clinical Sas Programmer jobs? Cities with the most Remote Clinical Sas Programmer job openings:
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Remote Clinical Sas Programmer jobs near you
Infographic showing various Remote Clinical Sas Programmer job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.
Associate Director, Statistical Programming

Associate Director, Statistical Programming

Verastem

Needham, MA • On-site, Remote

$165K - $190K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Associate Director, Statistical Programming


Job Duties:


  • Lead design and development SAS programs and the programming specifications for producing and validating CDISC ADaM datasets to support the generation of tables, figures and listings for clinical study report(s), FDA submission(s), and medical congress abstracts/posters/presentations;
  • Responsible for internal statistical programming deliveries across multiple clinical studies, as well as implementing process improvements and department initiatives;
  • Identify areas within clinical development functions where statistical programming tools and applications can enhance processes;
  • Perform quality control checks of advanced SAS code and output produced by other statistical programmers;
  • Work closely with clinical operations, data management and statisticians to develop infrastructure for timely and quality reporting of clinical trials to support regulatory requirements, and product launch activities;
  • Proactively identify issues and recommend solutions to optimize preparation, execution, reporting, and documentation of statistical programming activities;
  • Provide project management and technical guidance to ensure operational and technical excellence;
  • Liaise with vendors as needed to facilitate electronic data transfers and statistical programming support.

Requirements: Requirements include a Bachelor's or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus nine years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries; or in the alternative, a Master's degree or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus seven years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries.

Special Requirements:

If qualifying with bachelor's degree, must have the following:

  • 9 years of experience with SAS programing;
  • 9 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS;
  • 7 years of experience with CDISC SDTM and ADaM;
  • 7 years of experience with electronic FDA submission; and
  • 9 years of experience working in a clinical trial setting.

If qualifying with Master's degree, must have the following:

  • 7 years of experience with SAS programing;
  • 7 years of experience using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS;
  • 5 years of experience with CDISC SDTM and ADaM;
  • 5 years of experience with electronic FDA submission; and
  • 7 years of experience working in a clinical trial setting.


Work Location: Needham, MA

May work remotely from anywhere in U.S.

Multiple positions available. Applicants must have unrestricted authorization to work in the United States.

Salary: $165,000.00 - $190,000.00/year. 40 hours/wk full-time.

If interested and qualified for this position, please apply below.

Apply