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Senior Sas Developer Jobs in Edison, NJ (NOW HIRING)

Senior Scientist, Statistical Programming - Rahway, NJ: * Provide support to statistical ... Must possess expertise in SAS and clinical trial programming including data steps, procedures, SAS ...

The Senior Statistical Programmer plays a critical role in supporting clinical development programs ... Experience with SAS Life Science Analytics Framework (SAS LSAF) is preferred. Technical Skills ...

Senior Statistical Programmer The Senior Statistical Programmer will provide comprehensive ... Expertise in Base SAS, SAS/STAT, SAS/GRAPH, Reporting and Graphical Procedures, Macro, and SAS ...

Showing results 21-40

Senior Sas Developer information

See Edison, NJ salary details

$44

$66

$85

How much do senior sas developer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for senior sas developer in Edison, NJ is $66.37, according to ZipRecruiter salary data. Most workers in this role earn between $53.12 and $75.53 per hour, depending on experience, location, and employer.

What is a Senior SAS developer?

Senior SAS Developers are experienced professionals who specialize in using SAS (Statistical Analysis System) software to analyze complex data, develop statistical models, and create automated data processing solutions. They often design, program, test, and implement data-driven applications while ensuring data quality and integrity. These roles typically involve collaborating with business stakeholders, mentoring junior developers, and optimizing existing SAS programs for performance and efficiency.

What are some common challenges faced by senior SAS developers when working on large-scale data projects?

Senior SAS Developers often encounter challenges such as managing complex data integration tasks, optimizing code for performance with large data sets, and ensuring data quality and security. Collaborating with cross-functional teams—like data analysts, business stakeholders, and IT staff—requires strong communication skills to translate business requirements into efficient SAS solutions. Additionally, staying updated with new SAS features and regulatory compliance standards can be crucial for delivering successful outcomes.

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

To thrive as a Senior SAS Developer, you need advanced proficiency in SAS programming, data analysis, and statistical modeling, often supported by a degree in computer science, statistics, or a related field. Expertise in SAS Base, SAS Macro, SQL, and familiarity with data management tools and platforms like Teradata or Oracle are typically required, along with relevant certifications such as SAS Certified Advanced Programmer. Strong problem-solving, communication, and leadership skills help you effectively manage projects and collaborate with cross-functional teams. These skills ensure accurate data solutions, efficient process automation, and successful project delivery in complex data environments.

What is the difference between Senior Sas Developer vs Data Analyst?

AspectSenior Sas DeveloperData Analyst
Required CredentialsBachelor's in Computer Science or related field, SAS certificationsBachelor's in Statistics, Data Science, or related field, often with SAS or SQL certifications
Work EnvironmentDevelops and maintains SAS programs, works in IT or analytics teamsAnalyzes data, creates reports, collaborates with business units
Industry UsageFinance, healthcare, pharmaceuticals, and tech companiesRetail, marketing, finance, healthcare, and consulting firms

While both roles involve working with data and SAS tools, a Senior SAS Developer primarily focuses on developing and maintaining SAS applications and programs, often within IT teams. In contrast, a Data Analyst interprets data, creates reports, and provides insights to support business decisions. The roles overlap in data handling and SAS knowledge but differ in scope and primary responsibilities.

What are popular job titles related to Senior Sas Developer jobs in Edison, NJ?

For Senior Sas Developer jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Senior Sas Developer jobs in Edison, NJ look for?

The top searched job categories for Senior Sas Developer jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for Senior Sas Developer jobs?

Cities near Edison, NJ with the most Senior Sas Developer job openings:

Infographic showing various Senior Sas Developer job openings in Edison, NJ as of August 2026, with employment types broken down into 83% Full Time, 5% Part Time, and 12% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $138,059 per year, or $66.4 per hour.

Senior Scientist, Statistical Programming, Late-Stage Oncology (Remote)

MSD Malaysia

Rahway, NJ • On-site

$117 - $184/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago


Key responsibilities

  • Support statistical programming activities for late-stage drug/vaccine clinical development projects, including development and execution of analysis and reporting deliverables.

  • Design and maintain statistical datasets to support multiple stakeholder groups and serve as the statistical programming point of contact throughout the product lifecycle.

  • Coordinate activities of a global programming team, ensure timely and high-quality deliverables, and participate in departmental strategic initiatives.


Job description

## Senior Scientist, Statistical Programming, Late-Stage Oncology (Remote)Applyremote type: Remotelocations: USA - Pennsylvania - North Wales (Upper Gwynedd): USA - New Jersey - Rahwaytime type: Full timeposted on: Posted Todaytime left to apply: End Date: September 19, 2026 (30+ days left to apply)job requisition id: R412092**Job Description**In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.**Responsibilities:**This position supports statistical programming activities for late-stage drug/vaccine clinical development projects. This may include leadership of one or more projects. Accountability predominantly includes the development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.The position is a key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high-quality deliverables.For assigned projects the position serves as the statistical programming point of contact and knowledge holder through the entire product lifecycle.**Primary Activities:*** Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices* Maintain and manage a project plan including resource forecasting* Coordinate the activities of a global programming team that includes outsource provider staff* Membership on departmental strategic initiative teams.**Skills****Education and Minimum Requirement:*** BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years SAS programming experience in a clinical trial environment **OR*** MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 3 years SAS programming experience in a clinical trial environment**Department Required Skills and Experience:*** Effective interpersonal skills and ability to negotiate and collaborate effectively* Effective written, oral, and presentation skills* Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)* A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders**Position Specific Required Skills and Experience:*** Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise* Designs and develops complex programming algorithms* Ability to comprehend analysis plans which may describe methodology to be programmed; an understanding of statistical terminology and concepts* Familiarity with clinical data management concepts* Experience in CDISC and ADaM standards* Experience ensuring process compliance and deliverable quality* Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices* Ability to anticipate stakeholder requirements**Preferred Skills and Experience:*** Demonstrated experience with advanced programming languages such as R (including Shiny) and/or Python; familiarity with the application of Generative AI and emerging technologies within statistical programming pipelines is highly desirable.* Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)* US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables* Experience assuring programming consistency across protocols and projects, directing the program development effort of other programmers; experience as a programming mentor* Ability and interest to work across cultures and geographies* Ability to complete statistical programming deliverables through the use of global outsource partner programming staff* Experience developing and managing a project plan using Microsoft Project or similar package* Active in professional societies* Experience in process improvement* Demonstrated proficiency in steering statistical programming deliverables post-DBL, ensuring absolute data integrity of unblinded data.* Strong capability to operate efficiently in high-pressure environments, swiftly addressing emergent post-DBL challenges through decisive stakeholder communication and rapid technical resolution.BARDS2020eligibleforERPSPjobsVETJOBSEBRG**Required Skills:**Clinical Development, Clinical Trials, Data Management, Data Modeling, Emerging Technologies, Leadership, Numerical Analysis, Outcomes Research, Pressure Management, Project Leadership, Project Management, Project Planning, Stakeholder Relationship Management, Statistical Programming**Preferred Skills:**Open Source Technologies, Open Source Tools, Python (Programming Language), R Programming, R ShinyCurrent Employees apply HERECurrent Contingent Workers apply HERE**US and Puerto Rico Residents Only:**Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA SupplementWe are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State ActsThe salary range for this role is$117,000.00 - $184,200.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.**San Francisco Residents Only:** We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance**Los Angeles Residents Only:** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance**Search Firm Representatives Please Read Carefully** Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.**Employee Status:**Regular**Relocation:**Domestic**VISA Sponsorship:**Yes**Travel Requirements:**10%**Flexible Work Arrangements:**Remote**Shift:**Not Indicated**Valid Driving License:**No**Hazardous Material(s):**n/a**Job Posting End Date:**09/19/2026**\*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.**Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. #J-18808-Ljbffr