ZipRecruiter

Log In

1

Sas Programming Manager Jobs (NOW HIRING)

Clinical Ink

SAS Programmer

... Management team based remotely across the United States! This individual will develop and implement data export programming based on mapping requirements as well as develop clinical data report ...

New

Saxon Global

SAS Developer

Charlotte, NC

S., providing enhanced IT consulting and engineering solution services for past 16 years. Saxon ... Hands-on experience using SAS development and tuning. 7+ years of experience in managing large ...

Sonsoft Inc

SAS Developer

Charlotte, NC

Access Data, Managing Data , Handling Errors, Macro Processing , Advanced Programming Techniques. * Strong knowledge of SAS architecture. * Knowledge of Efficient ways to flow huge data from various ...

Sonsoft Inc

SAS Developer

Charlotte, NC

Access Data, Managing Data , Handling Errors, Macro Processing , Advanced Programming Techniques.. * Strong knowledge of SAS architecture.. * Knowledge of Efficient ways to flow huge data from ...

MSD

Senior Scientist, Statistical Programming

North Wales, PA · On-site +1

$117K - $184K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

SAS). * Write code for Tables, Listings and Figures (TLFs) macros and implement statistical ... Maintain and manage a project plan including resource forecasting. * Coordinate the activities of a ...

SA Technologies Inc.

SAS Programmer

Philadelphia, PA · On-site

Receive and review non-client standard client file specifications from Data Manager / Project ... Experience with DB programming is a plus. Ability to work in a rapidly changing and fast-paced ...

previous page

Showing results 41-60

All JobsSas Programming JobsSas Programming Manager Jobs

Sas Programming Manager information

See salary details

$14

$49

$79

How much do sas programming manager jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for sas programming manager 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 is a SAS programming manager?

SAS Programming Managers are professionals who oversee teams of SAS programmers, typically within the pharmaceutical, clinical research, or data analytics industries. Their responsibilities include project management, team leadership, and ensuring quality standards for statistical programming deliverables. They coordinate with other departments, manage timelines, and ensure that all data analysis and reporting using the SAS software adhere to regulatory and organizational requirements.

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

To thrive as a SAS Programming Manager, you need advanced SAS programming expertise, a solid background in statistics or data analysis, and typically a degree in a quantitative field with relevant management experience. Familiarity with clinical data management systems, regulatory standards (such as CDISC), and tools like SAS Base, Macro, and SQL is essential. Strong leadership, project management, and communication skills help you effectively lead teams and collaborate across departments. These competencies ensure the delivery of high-quality data outputs, regulatory compliance, and the successful management of complex projects.

What is the difference between Sas Programming Manager vs Sas Developer?

AspectSas Programming ManagerSas Developer
CredentialsBachelor's or Master's in Computer Science, Statistics, or related field; SAS certifications often preferredBachelor's in similar fields; SAS certifications beneficial
Work EnvironmentLeads teams, manages projects, collaborates with stakeholdersDevelops SAS programs, analyzes data, implements solutions
Industry UsageUsed in healthcare, finance, pharma for project oversightUsed across industries for data analysis and reporting
Search & ComparisonOften compared for leadership roles in SAS programmingFocuses on coding and data analysis tasks

The Sas Programming Manager oversees SAS projects and manages teams, while the Sas Developer primarily focuses on coding and data analysis. Both roles require SAS skills and certifications, but the manager role involves leadership and project management responsibilities, whereas the developer role emphasizes technical programming tasks.

What are some typical challenges faced by a SAS programming manager when leading a team of programmers in a clinical research setting?

A SAS Programming Manager in clinical research often encounters challenges such as balancing tight project timelines with data quality standards, coordinating cross-functional communication between statisticians, data managers, and regulatory teams, and ensuring team members stay updated on evolving industry regulations (like CDISC standards). Managing a diverse team with varying experience levels also requires strong mentorship and effective delegation to ensure consistent deliverables. Addressing these challenges proactively helps maintain project momentum and fosters professional growth within the team.
More about Sas Programming Manager jobs

What cities are hiring for Sas Programming Manager jobs?

Cities with the most Sas Programming Manager job openings:

What are the most commonly searched types of Sas Programming jobs?

The most popular types of Sas Programming jobs are:

What states have the most Sas Programming Manager jobs?

States with the most job openings for Sas Programming Manager jobs include:

What job categories do people searching Sas Programming Manager jobs look for?

The top searched job categories for Sas Programming Manager jobs are:

Sas Programming Manager jobs near you
Infographic showing various Sas Programming Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

Associate Director, Statistical Programming

Alnylam Pharmaceuticals

Cambridge, MA • On-site

$181K - $244K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago

Job description

The Associate Director, Statistical Programming is responsible for statistical programming activities in support of clinical trials including technical and project leadership overseeing the quality and timely delivery of all statistical programming deliverables for studies or for a submission. He/she ensures the team develops, maintains, validates and runs quality SAS programs that access, visualize, analyze, and report clinical trial data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. While SAS expertise is required, experience with R programming, particularly data visualization and exploratory analysis is strongly preferred.
Summary of Key Responsibilities
  • Provides technical and/or operational leadership in the delivery of high quality and timely statistical programming for clinical studies, drug programs, and/or in support of NDA submissions.
  • Works closely with Biostatistics to implement statistical analysis of clinical trial data, working closely on the development and validation of CDISC ADaM specifications and datasets, and TLFs for analyses to support regulatory, medical affairs, and market access needs.
  • Works closely with Data Management on cross-functional data review and the development and validation of CDISC SDTM specifications and datasets and define packages, may also support Drug Safety to support safety data review and reporting needs, and/or Clinical Pharmacology to support their dataset creation and analytic needs.
  • Manages internal and vendor statistical programming support; Maintains strong collaboration and governance with preferred vendors.
  • Writes SAS and R code that produces or validates tables, listings, figures and analysis datasets, in support of clinical studies or complex integrated analyses for submission.
  • Performs, plans and coordinates project work to ensure timely, quality delivery across multiple projects, or across a drug program.
  • Writes specifications to describe programming needs, including development and maintenance of complex / ADaM specifications and reviewer guides.
  • May lead the creation and validation of global macros or systems that streamline repetitive operations to increase programming efficiency.
  • Provides input into, or leads general standardization efforts (e.g., CRFs, query checks, standard statistical programs, data presentations).
  • Leads efforts to develop programming processes consistent with industry best practices.
  • Reviews and provides expert input to DMP, eCRF specs, and other clinical data management documents; Reviews and provides expert input to statistical analysis plans and other related documents.
  • Partners with or oversees CROs or Programming vendors to perform any of the above tasks.

Qualifications
  • At least 10 years' industry (Pharmaceutical, Biotech, CRO) SAS programming experience or equivalent;
  • Experience as a Programming manager (FTEs, Functional Service Providers or vendors);
  • Experience leading programming teams in support of clinical trials to report the results of clinical trials, integrate analyses across a program, or prepare data/analysis for electronic NDA or BLA submission;
  • Experience in constructing technical programming specifications and producing complex, validated SAS programs;
  • Demonstrated experience in working with CDISC standards, including SDTM, and ADaM, and Define xml;
  • Proficiency in understanding of statistical programming environments, processes, procedures, and roles;
  • Excellent knowledge of SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL with a demonstrated mastery of SAS/STAT procedures;
  • Hands-on experience with R programming for clinical trial data analysis, reporting, and regulatory submissions.
  • Knowledge of R packages and frameworks commonly used in clinical development, Posit Workbench (RStudio Server), Posit Package Manager, and enterprise R environments.
  • Experience developing SOPs, Standards or implement programming best practices;
  • Experience overseeing vendors in the delivery of quality programming support;
  • Excellent written and oral communication and organizational skills required;
  • Bachelor's Degree required, master's degree Preferred, in areas of computer science, statistics, mathematics or information sciences.
  • Clear alignment with Alnylam Core Values:
    • Commitment to People
    • Innovation and Discovery
    • Sense of Urgency
    • Open Culture
    • Passion for Excellence

#LI-AB1 #LI-Hybrid
U.S. Pay Range
$181,100.00 - $244,900.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

Apply