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Pharmaceutical Sas Programmer Jobs in Raleigh, NC

IQVIA

Senior Statistical Programmer

Durham, NC

$88K - $220K/yr

Or equivalent experience * 4 - 8 years of SAS programming working experience in the pharmaceutical industry. * Good SAS programming skills and attention to details * Demonstrated knowledge of ...

IQVIA

Senior Statistical Programmer

Durham, NC · On-site

$88K - $220K/yr

Or equivalent experience * 4 - 8 years of SAS programming working experience in the pharmaceutical industry. * Good SAS programming skills and attention to details * Demonstrated knowledge of ...

micro1 AI

Director of Biostatistics

Raleigh, NC · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

Cary, NC · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

micro1 AI

Director of Biostatistics

Durham, NC · Remote

$60 - $100/hr

MS or PhD in biostatistics, statistics, or epidemiology. * 4+ years of experience in pharmaceutical ... Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological ...

MMS

Senior Biostatistician - Remote (US)

Raleigh, NC · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... Strong programming and logic skills (working knowledge of SAS) * Ability to apply drug development ...

INC Research

Senior Biostatistician

Raleigh, NC · On-site

... for the world's pharmaceutical, biotech and medical device industries. We do this across six ... SAS programming. Excellent knowledge of statistical theory including experimental design ...

INC Research

Senior Biostatistician

Raleigh, NC

... for the world's pharmaceutical, biotech and medical device industries. We do this across six ... SAS programming. Excellent knowledge of statistical theory including experimental design ...

IQVIA

Senior Epidemiological Programmer RWE

Durham, NC · On-site

$88K - $220K/yr

Demonstrated proficiency in advanced statistical programming using SAS and/or R, macros, SQL * Prior pharmaceutical experience and advanced knowledge of observational research study design and ...

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Pharmaceutical Sas Programmer information

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How much do pharmaceutical sas programmer jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for pharmaceutical sas programmer in Raleigh, NC is $47.64, according to ZipRecruiter salary data. Most workers in this role earn between $33.41 and $59.81 per hour, depending on experience, location, and employer.

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.

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 are the most commonly searched types of Pharmaceutical Sas Programmer jobs in Raleigh, NC?

The most popular types of Pharmaceutical Sas Programmer jobs in Raleigh, NC are:

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Pharmaceutical Sas Programmer jobs near you
Infographic showing various Pharmaceutical Sas Programmer job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $99,083 per year, or $47.6 per hour.

Senior Statistical Programmer

IQVIA

Durham, NC

$88K - $220K/yr

Full-time

Re-posted 6 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

Essential Functions of the Job (Key responsibilities)

  • Conduct statistical programming work of clinical data using SAS Software.
  • Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.
  • Generate analysis datasets according to CDISC standard and SAP.
  • Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct adhoc analyses.
  • Validate programs and associated results produced by other programming colleagues.
  • Participate in TLF shell preparation and review, and assist statistician for SAP preparation.
  • Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.
  • Learn, and implement Incyte standard SAS macros for efficient analyses of clinical data supervised by Lead programmers.
  • Work independently to program for individual studies with minimum supervision.
  • Check that the validation summary reports are clean of errors and warnings, and show proper documentation of SAS programs.
  • Review individual study CDISC validation output.

Qualifications (Minimal acceptable level of education, work experience, and competency)

  • BA/BS degree in mathematics, statistics, computer science or health related field. Or equivalent experience
  • 4 - 8 years of SAS programming working experience in the pharmaceutical industry.
  • Good SAS programming skills and attention to details
  • Demonstrated knowledge of regulatory guidelines, including electronic submission standards.
  • Strong organizational, time management, communication, and project coordination and leadership skills.
  • Must be able to work well under timeline pressure.
  • Must be able to work on multiple tasks while coordinating others at the same time.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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