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Pharmaceutical Sas Programmer Jobs in Raleigh, NC

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 ...

WiTH Collective

Senior Statistical Programmer (Remote)

Cary, NC · On-site

$104.75 - $128/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... of SAS programming experience required. * R programming experience highly preferred. * 2 years of macro programming experience required. * At least 3 years of experience in the pharmaceutical ...

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

$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 ...

Gilead

Senior Manager, Statistical Programming

Raleigh, NC · On-site

$169K - $219K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Degree in Biostatistics/Computer Science or equivalent * 8+ years of pharmaceutical/CRO experience ... GCP, ICH) * Extensive experience with statistical programming using the SAS software including ...

Gilead

Senior Manager, Statistical Programming

Raleigh, NC

$169K - $219K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Degree in Biostatistics/Computer Science or equivalent * 8+ years of pharmaceutical/CRO experience ... GCP, ICH) * Extensive experience with statistical programming using the SAS software including ...

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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 14, 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 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.

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:

What are popular job titles related to Pharmaceutical Sas Programmer jobs in Raleigh, NC?

For Pharmaceutical Sas Programmer jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Pharmaceutical Sas Programmer jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Pharmaceutical Sas Programmer jobs?

Cities near Raleigh, NC with the most Pharmaceutical Sas Programmer job openings:

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 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $99,083 per year, or $47.6 per hour.

Director of Biostatistics

micro1 AI

Raleigh, NC • Remote

$60 - $100/hr

Part-time

Posted 8 days ago

Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
  2. Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
  3. Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
  4. Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
  5. Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
  6. Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.


Preferred Qualifications

  1. MS or PhD in biostatistics, statistics, or epidemiology.
  2. 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
  3. Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
  4. Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
  5. Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
  6. Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
  7. Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.


Compensation Structure

Compensation is output-based; experts are paid per task that meets the project specifications. The time required to complete work may vary depending on the expert’s experience and workflow. Minimum submission requirements apply. Experts must submit a minimum of tasks per week.


Start Timeline & Availability

We typically fill roles within 48 hours and are looking for experts ready to jump in right away. If selected, we expect you to start your first tasks within 24–48 hours of completing onboarding.

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