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Remote Clinical Sas Programmer Jobs (NOW HIRING)

ProKidney

Programming Contractor

The Statistical Programmer Contractor is responsible for developing, validating, and maintaining SAS programming deliverables to support clinical study analysis and reporting. This role collaborates ...

ProKidney

Programming Contractor

The Statistical Programmer Contractor is responsible for developing, validating, and maintaining SAS programming deliverables to support clinical study analysis and reporting. This role collaborates ...

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

Proficiency in all SAS language, procedures, and functions commonly used in clinical trial ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

LivaNova

Statistical Programmer II

$90K - $100K/yr

Collaborate with Statistics, Data Management, Clinical, and vendor teams to clarify requirements and resolve data or programming issues. * Develop, validate, and maintain SAS programs in accordance ...

BeiGene USA

(Senior) Principal Statistical Programmer

$144K - $189K/yr

Minimum 5+ years of clinical research and development programming experience using SAS. Expert-level knowledge and extensive hands-on experience with CDISC methodologies. Experience leading or ...

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Remote Clinical Sas Programmer information

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$19

$54

$80

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

As of Sep 2, 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 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?

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 does a remote clinical SAS programmer do?

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 are the key skills and qualifications needed to thrive as a remote clinical SAS programmer?

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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Remote Clinical Sas Programmer jobs near you
Infographic showing various Remote Clinical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% 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.

Programming Contractor

ProKidney

Remote

Full-time

Posted 12 days ago

Job description

Position Summary:The Statistical Programmer Contractor is responsible for developing, validating, and maintaining SAS programming deliverables to support clinical study analysis and reporting. This role collaborates closely with Biostatistics and other cross-functional team members to produce high-quality, compliant datasets, tables, listings, and figures while ensuring adherence to project timelines, SOPs, regulatory requirements, and CDISC standards.Responsibilities:Program and validate tables, listings, figures, and derived datasets using SAS.Develop SDTM and ADaM specs, datasets, and supporting documentation.Prepare and review mapping specifications, annotated case report forms (aCRF), define, SDRG, ADRG and other files needed in the submission.Perform quality control and validation activities for all programming deliverables.Collaborate with study team members to identify, investigate, and resolve data and output issues.Review study documents and provide input to improve programming quality, efficiency, and consistency.Maintain complete, accurate, and audit-/inspection-ready programming documentation.Communicate project status, risks, issues, and timeline impacts clearly to stakeholders.Other as assigned.Qualifications:Bachelor's degree required; Master's degree preferred in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.Minimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.Phase 3 and regulatory submission experience preferred.Strong SAS programming skills, with experience developing SDTM, ADaM, tables, listings, and figures.Strong knowledge of clinical trial processes, regulatory requirements, and programming documentation.High attention to detail, with strong analytical, problem-solving, and communication skills.Ability to work independently and manage multiple priorities in a deadline-driven environment.ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship. Salary: . Date posted: 08/21/2026
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About ProKidney

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

Winston-Salem, NC, US

Year founded

2019

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