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Pharmaceutical Sas Programmer Jobs (NOW HIRING)

EDETEK

Senior Statistical Programmer

Minimum of 5 years of experience in statistical programming within the pharmaceutical or clinical research industry. * Proficiency in SAS programming; experience with R and other statistical software ...

CareSet Systems

SAS Statistician

Houston, TX · On-site

$95K/yr

... pharmaceutical companies. CareSet also works with research arm DocGraph to create, maintain, and ... developer. You also don't just look at numbers and pass them on unexamined. You appreciate that ...

CareSet Systems

SAS Statistician

Houston, TX

$95K/yr

... pharmaceutical companies. CareSet also works with research arm DocGraph to create, maintain, and ... developer. You also don't just look at numbers and pass them on unexamined. You appreciate that ...

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How much do pharmaceutical sas programmer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for 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 are the key skills and qualifications needed to thrive as a pharmaceutical SAS programmer?

To thrive as a Pharmaceutical Sas Programmer, you need strong expertise in SAS programming, clinical data analysis, and a solid understanding of regulatory requirements, typically supported by a degree in statistics, computer science, or a related field. Familiarity with CDISC standards (such as SDTM and ADaM), exposure to clinical trial management systems, and SAS certifications are commonly expected. Attention to detail, problem-solving abilities, and effective communication skills help distinguish top performers in this role. These skills are essential for ensuring the accuracy, compliance, and clarity of clinical trial data submitted to regulatory authorities.

What is a pharmaceutical SAS programmer?

A Pharmaceutical SAS Programmer is responsible for analyzing clinical trial data using SAS software. They develop, validate, and manage programs to generate statistical outputs like tables, listings, and figures for regulatory submissions. Their role ensures compliance with industry standards such as CDISC (SDTM and ADaM) and FDA guidelines. They collaborate with statisticians, data managers, and regulatory teams to ensure accurate data reporting and support drug development processes.

What types of projects or responsibilities can I expect as a pharmaceutical SAS programmer?

As a Pharmaceutical Sas Programmer, you will primarily be tasked with writing and validating programs to analyze clinical trial data, generate tables, listings, and figures (TLFs), and ensure outputs meet regulatory standards. You may collaborate closely with biostatisticians, clinical data managers, and other programmers to interpret datasets, implement statistical analysis plans, and troubleshoot issues in data processing. The work is typically project-based, often requiring you to prioritize multiple studies or phases simultaneously and adhere to tight deadlines. This role offers exposure to the full drug development lifecycle and provides valuable experience for advancing into senior programming, data management, or biostatistics positions.

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Pharmaceutical Sas Programmer jobs near you
Infographic showing various Pharmaceutical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

Senior Statistical Programmer

EDETEK

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 27 days ago

Job description

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team. As a leader in data analytics, we are dedicated to providing innovative solutions to our clients in the pharmaceutical and healthcare sectors. In this pivotal role, you will leverage your expertise in statistical programming to ensure the integrity and quality of our data analyses. You will work closely with biostatisticians, clinical data managers, and other cross-functional teams to develop and execute statistical analyses that drive decision-making processes. The ideal candidate will have a strong background in programming languages such as SAS and R, as well as a deep understanding of clinical trial methodology and regulatory requirements. This position offers the opportunity to collaborate on high-impact projects, mentor junior programmers, and contribute to the development of our programming standards. If you are passionate about turning data into actionable insights and have a proven track record in advanced statistical programming, we invite you to apply and become a crucial part of our innovative team at Edetek.
Essential Functions and Responsibilities
  • Develop and validate SAS programs to generate SDTM, ADaM datasets, tables, listings, and figures for clinical trial data.
  • Collaborate with biostatisticians and data managers to understand project requirements and statistical analysis plans.
  • Perform data manipulation and statistical analyses using appropriate programming techniques.
  • Develop, review and critique programming specifications and outputs to ensure accuracy and compliance with standards.
  • Mentor and provide guidance to junior statistical programmers to enhance their skills and productivity.
  • Participate in the development and implementation of programming standards and best practices.
  • Contribute to regulatory submissions by preparing documentation and providing support during audits.

Requirements
  • Bachelor's degree in Statistics, Biostatistics, Mathematics, or a related field; Master's degree preferred.
  • Minimum of 5 years of experience in statistical programming within the pharmaceutical or clinical research industry.
  • Proficiency in SAS programming; experience with R and other statistical software is a plus.
  • Strong understanding of clinical trial design and regulatory requirements for statistical analysis.
  • Experience with data management processes and data validation techniques.
  • Excellent problem-solving skills and attention to detail.
  • Strong communication skills, both verbal and written, to effectively collaborate with cross-functional teams.

Benefits
Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees.
  • Choice of comprehensive Medical, Vision and Dental Insurance plans
  • Paid vacation time and sick days
  • Corporate holidays annually
  • Participation in the 401K Plan
  • Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc.
  • Health Advocate and Employee Assistance Program

Location:
This is a remote position, and we are open to candidates based in the United States, Bulgaria, Romania, Poland, India, Ukraine, Sri Lanka, Philippines.
Equal Opportunity Employer Statement
EDETEK is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment on the basis of an individual's race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Whenever possible, the company makes reasonable accommodations for qualified individuals with disabilities to the extent required by law.
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About Edetek

Sourced by ZipRecruiter

Industry

Software development

Company size

201 - 500 Employees

Headquarters location

Princeton, NJ, US

Year founded

2009

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