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Principal Sas Programmer Jobs (NOW HIRING)

IQVIA, Inc.

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for mid-July Position Summary We are seeking ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * In-depth knowledge ...

IQVIA, Inc.

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Position Summary We are seeking a Principal Statistical Programmer to provide full end-to-end ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * In-depth knowledge ...

Principal Software

SAS Grid Admin

Oakland, CA · On-site

$80/hr

Bachelor's degree in a technical field such as computer science, computer engineering or related field required Nice to Haves: * Experience with SAS/BASE, SAS/SQL, SAS/MACROS, SAS/GRAPH, SAS/STAT

IQVIA

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

IQVIA

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

IQVIA

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

Cytel

Principal Biostatistician FSP

Cambridge, MA · On-site +1

An experienced Principal Biostatistician with a passion for clinical development and analysis ... SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with ...

Principal Software

SAS Grid Admin

Oakland, CA

$80/hr

Bachelor's degree in a technical field such as computer science, computer engineering or related field required Nice to Haves: * Experience with SAS/BASE, SAS/SQL, SAS/MACROS, SAS/GRAPH, SAS/STAT

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Principal Sas Programmer information

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How much do principal sas programmer jobs pay per month?

As of Jun 19, 2026, the average monthly pay for principal sas programmer in the United States is $14,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $12,291.67 and $15,416.67 per month, depending on experience, location, and employer.

What are the typical responsibilities and day-to-day tasks for a Principal SAS Programmer?

As a Principal SAS Programmer, your daily tasks often include developing and validating statistical programs, overseeing the creation of datasets, tables, listings, and figures (TLFs) for clinical studies, and ensuring data quality and compliance with regulatory standards. You’ll collaborate with statisticians, data managers, and clinical teams to understand study requirements and deadlines. Additionally, you may mentor junior programmers, provide programming guidance, and help resolve technical challenges within the team. This role offers a mix of independent programming work and cross-departmental collaboration, making it both technically challenging and highly impactful within the organization.

What is a Principal SAS Programmer job?

A Principal SAS Programmer is a senior-level professional responsible for leading statistical programming activities in clinical trials or other data-driven industries. They design, develop, validate, and maintain complex SAS programs to analyze and report data, ensuring compliance with regulatory guidelines. Additionally, they collaborate with biostatisticians, data managers, and clinical teams to support study objectives. Their role often includes mentoring junior programmers and optimizing programming workflows for efficiency and accuracy.

Are SAS programmers in demand?

SAS programmers are in demand in industries such as healthcare, finance, and pharmaceuticals that rely on data analysis and reporting. Strong skills in SAS, along with knowledge of data management and statistical analysis, can improve job prospects, especially for those with certifications and experience in analytics environments.

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

To thrive as a Principal SAS Programmer, you need advanced expertise in SAS programming, statistical analysis, and clinical data management, often gained through a degree in statistics, computer science, or a related field. Familiarity with industry-standard tools like SAS Base, SAS Macro, and regulatory submission standards such as CDISC (SDTM, ADaM), as well as relevant certifications, is highly valued. Leadership, problem-solving, and effective communication are essential soft skills for managing projects and collaborating with cross-functional teams. These competencies are crucial for ensuring data integrity, regulatory compliance, and the successful delivery of complex clinical projects.

What is the average salary for a SAS programmer?

The average salary for a SAS programmer varies by experience and location but typically ranges from $70,000 to $110,000 annually. Senior SAS programmers with advanced skills and certifications can earn higher salaries, especially in industries like pharmaceuticals and finance where data analysis is critical.

How much do SAS programmers make?

SAS programmers typically earn between $70,000 and $120,000 annually, depending on experience, location, and industry. Senior roles or those with advanced skills in data analysis and programming may have higher salaries, especially in healthcare, finance, or pharmaceutical sectors.

What is the salary of principal statistical programmer in Eli Lilly?

The salary for a Principal Statistical Programmer at Eli Lilly typically ranges from $110,000 to $150,000 annually, depending on experience, location, and qualifications. This role often requires proficiency in SAS programming and knowledge of clinical trial data analysis.
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Principal Sas Programmer jobs near you
Infographic showing various Principal Sas Programmer job openings in the United States as of June 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 100% In-person job distribution, with an average salary of $174,000 per year, or $83.7 per hour.

Senior/Principal Clinical Programmer

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Full-time

Posted 26 days ago

Job description

Job Title: Principal Clinical Programmer
Job Code: CDM0016
Department Name: Clinical Data Management
Reports to Title: Manager or above
Job Summary:
The Principal Clinical Programmer is a member of the Data Management team and serves as a subject matter expert for Clinical Data Programming, Reporting, Process, and technology. Accountable for the quality and delivery of the Data Management programming, reporting and visualization, standard, and exception data listings across studies. Scope of work includes oversight and expertise in the design, development, and validation of programs, standard and adhoc reports, standard and exception data listings, and visualizations to support ongoing data review activities, achieve critical study milestones, and gain data insights into our clinical studies. The position requires good understanding of programming methods and techniques, critical thinking, and complex problem-solving skills. This position will require strong collaboration in working with other members of the Biostatistics and Data Management, external CRO partners, and other stakeholders.
Responsibilities:
  • Serve as a subject matter expert and provide expertise for Database programming, Reporting, and Technology and optimize the use of J-Review, ETL, SAS tools, and others to support business needs.
  • Manage the quality of the data management clinical database programming deliverables including edit checks programming, complex reports, and listings; patient profiles, subject narratives, exception listings, dose modification reports, and other adhoc reports using JReview & SAS as part of standard data validation and reporting package for clinical studies.
  • Develop and/or provide oversight on the programming specifications for the data validation and reporting deliverables; code, test, and document deliverables conforming to programming standards, data quality and governance, and validation policies.
  • Partner with internal and external stakeholders to ensure timely delivery of data management programming, EDC database, external data, data management programming of reports and listings including the use of visualization tools.
  • Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities.
  • Develop standard programs, templates, reports, data listings, discrepancy reports, and patient profiles to facilitate in the ongoing review of clinical data during study conduct and study closeout.
  • Build, test, and scale-up programs for data validation derivation procedures, data reports, listings, and SAS on Demand relational database extracts for operational use, identification of data outliers, quality inconsistencies, and preparation for analysis.
  • Provide technical guidance and direct programming tasks for Medical Coding activities.
  • Provide Clinical Programming expertise and support for critical and time-sensitive study milestones including interim analysis, and database lock activities.
  • Perform ETL tasks, enhancements, validation, and maintenance of the programs and templates on an ongoing basis.
  • Perform QC, lead unit testing activities, develop validation scripts for user acceptance, manage and execute programs and dry runs as needed, and resolve programming issues proactively.
  • Develop and maintain mapping, and program specifications for standard reports, listings, and visualizations.
  • Maintain database programming checklists and trackers to ensure conformance of high-quality deliverables with the study data validation and reporting package.
  • Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.
  • Participate in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.

Experience:
  • Minimum of 5 years database programming experience and data validation programming in the device/pharmaceutical/CRO industry.
  • Expertise in Clinical Programming, methods, and techniques
  • Expertise in using standard reporting and data visualization tools including JReview, and SAS tools.
  • Knowledge of industry standard clinical technologies including CTMS, EDC (RAVE, InForm)
  • Knowledge of CDISC data standards.
  • Knowledge and understanding of relational databases.
  • Clinical Programming, Project Management, and Technical Expertise
  • Knowledge of logical data design and data mapping
  • Knowledge of reporting and data visualization tools: JReview, Spotfire, SAS suite and ETL technology
  • Experience with programming development, validation, execution, maintenance, documentation, and archival of clinical data for regulatory submission is required.
  • Proficient in industry standards, medical terminology, and clinical trial methodologies.

Education:
  • Bachelor of Science degree in Computer Science, Mathematics, or related area with relevant experience
  • Other degrees and certifications considered if commensurate with related data management experience

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