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Lead Sas Programmer Jobs (NOW HIRING)

Apex Informatics

Mainframe Lead/Manager

What You'll Do: lead a team of mainframe and SAS developers. Strong in SQL and Teradata Transitioning from a technical role: You possess a strong technical background and have successfully ...

Apex Informatics

Mainframe Lead/Manager

What You'll Do: lead a team of mainframe and SAS developers. Strong in SQL and Teradata Transitioning from a technical role: You possess a strong technical background and have successfully ...

Fortrea

Senior Statistical Programmer

San Jose, CA · Remote

Perform the role of the Lead Statistical Programmer. * Plan, execute and oversee all programming ... Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM ...

PSI CRO

Principal Statistician

Durham, NC

Lead teams of SAS programmers and/or statisticians on the project level Qualifications * MSc in Statistics or equivalent * Expert knowledge and understanding of the statistical principles, concepts ...

PSI CRO

Principal Statistician

Durham, NC

Lead teams of SAS programmers and/or statisticians on the project level Qualifications * MSc in Statistics or equivalent * Expert knowledge and understanding of the statistical principles, concepts ...

PSI CRO

Principal Statistician

Lead teams of SAS programmers and/or statisticians on the project level Qualifications * MSc in Statistics or equivalent * Expert knowledge and understanding of the statistical principles, concepts ...

PSI CRO

Principal Statistician

Durham, NC · On-site

Lead teams of SAS programmers and/or statisticians on the project level Qualifications * MSc in Statistics or equivalent * Expert knowledge and understanding of the statistical principles, concepts ...

PSI CRO

Principal Statistician

Durham, NC · On-site +1

Lead teams of SAS programmers and/or statisticians on the project level Qualifications * MSc in Statistics or equivalent * Expert knowledge and understanding of the statistical principles, concepts ...

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Lead Sas Programmer information

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How much do lead sas programmer jobs pay per hour?

As of May 31, 2026, the average hourly pay for lead sas programmer in the United States is $54.96, according to ZipRecruiter salary data. Most workers in this role earn between $43.27 and $68.75 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Lead SAS Programmer, and why are they important?

To thrive as a Lead SAS Programmer, you need advanced proficiency in SAS programming, statistical analysis, and a background in fields like statistics, computer science, or life sciences. Familiarity with tools such as SAS Base, SAS Macros, and clinical data management systems, as well as certifications like SAS Certified Advanced Programmer, are typically required. Strong leadership, problem-solving, and communication skills help you guide teams, manage projects, and liaise with cross-functional stakeholders. These skills are vital for ensuring data quality, regulatory compliance, and team effectiveness in complex data-driven environments.

What are some common challenges faced by a Lead SAS Programmer and how can they be addressed?

Lead SAS Programmers often encounter challenges such as managing complex data integration tasks, ensuring data quality, and coordinating with cross-functional teams. Balancing project deadlines while maintaining compliance with industry standards (such as CDISC in clinical trials) can be demanding. Effective communication, strong project management skills, and staying updated with the latest SAS tools and regulations are key strategies for addressing these challenges. Collaborating closely with statisticians, data managers, and junior programmers also helps in streamlining workflows and resolving issues promptly.

What are Lead SAS Programmers?

Lead SAS Programmers are advanced analytics professionals who oversee the design, development, and implementation of data analysis and reporting solutions using SAS (Statistical Analysis System) software. They often manage teams of programmers, coordinate project activities, and ensure that statistical programming deliverables meet regulatory and client requirements, particularly in industries like pharmaceuticals and clinical research. Their responsibilities also include mentoring junior staff, reviewing code for quality and accuracy, and serving as key technical experts throughout the project lifecycle.

What is the difference between Lead Sas Programmer vs SAS Developer?

AspectLead Sas ProgrammerSAS Developer
CredentialsTypically requires a bachelor's degree in computer science or related field; experience in SAS programming; sometimes certifications like SAS Certified Data ScientistUsually requires a bachelor's degree; SAS certification is common but not always mandatory
Work EnvironmentLeads projects, manages teams, and collaborates with stakeholders in healthcare, finance, or pharma industriesFocuses on developing and maintaining SAS programs within project teams, often under supervision
Employer & Industry UsageUsed in industries requiring data analysis and reporting, such as healthcare, finance, and pharmaceuticalsCommonly employed in similar industries for data analysis and reporting tasks

The main difference between a Lead Sas Programmer and a SAS Developer lies in their responsibilities and seniority. The Lead Sas Programmer oversees projects, manages teams, and interacts with stakeholders, while the SAS Developer primarily focuses on coding and implementing SAS solutions. Both roles require similar credentials and are vital in data-driven industries.

More about Lead Sas Programmer jobs
What states have the most Lead Sas Programmer jobs? States with the most job openings for Lead Sas Programmer jobs include:
What job categories do people searching Lead Sas Programmer jobs look for? The top searched job categories for Lead Sas Programmer jobs are:
Lead Sas Programmer jobs near you
Infographic showing various Lead Sas Programmer job openings in the United States as of May 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Temporary. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $114,323 per year, or $55 per hour.
Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must

Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must

Cytel

Cambridge, MA • On-site, Remote

Full-time

Posted 20 days ago

Job description

Job Description
Sponsor-dedicated:
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview:
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Early or Late-stage clinical trials. This role is Hybrid office based in PA (Preferred) OR NJ.
Our values
  • We believe in applying scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
  • We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities
How you will contribute:
  • Generating and validating statistical programming deliverables (SDTM, ADAM, TFL's) in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas
  • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
  • Production and QC / validation programming
  • Generating complex ad-hoc reports utilizing raw data
  • Applying strong understanding/experience of Efficacy analysis
  • Creating and reviewing submission documents and eCRTs
  • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
  • Performing lead duties when called upon
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change

Qualifications
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
  • Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
  • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a master's degree or above.
  • Having experience/expertise working on Early Development studies. Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters).
  • Develop and validate global programming standards for ADaM datasets.
  • Develop and validate global programming standards for efficacy analysis, safety analysis and reporting.
  • Design and develop complex programming algorithms.
  • Experience in one or more of the following will be preferred: R, SPlus, NonMem.
  • Assist project teams in creating SDTM deliverables for Analysis and Reporting (A&R) and submission.
  • Support project teams in preparing submission deliverables including use of Pinnacle 21 Enterprise.
  • Up-versioning activities to specific versions of SDTM.
  • Experience supporting Oncology studies would be a plus.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Knowledge of submission standards CDISC SDTM, Define.XML, SDRG, aCRF.
  • Strong QC / validation skills.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.
  • Excellent analytical & troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

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