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Sas Programmer Contract Jobs in Springfield, NJ (NOW HIRING)

Sonsoft Inc

MS Data Integration

New York, NY · On-site

Excellent technical skills in SAS system and application development. SDTM. * Proven experience in ... Additional Information Note:- This is a Contract job opportunity for you. Only Only US Citizen ...

Sonsoft Inc

MS Data Integration

New York, NY · On-site

Excellent technical skills in SAS system and application development. SDTM. * Proven experience in ... Additional Information Note:- This is a Contract job opportunity for you. Only Only US Citizen ...

Navtech

ETL Data Analyst

Whitehouse Station, NJ · On-site

Whitehouse Station, NJ Position Type: Long Term Contract Responsibilities: * Strong skills in ... SQL etc), programming (XML, Javascript, or ETL frameworks). * Knowledge of statistics and ...

Sonsoft Inc

Data Wrangler

New York, NY · On-site

Knowledge on SAS & modelling or predictive analysis Using analytical programming languages PYSpark ... This is a Contract job for you * Only US Citizen, Green Card Holder, TN Visa, GC-EAD , H4-EAD & L2 ...

Sonsoft Inc

Data Wrangler

New York, NY · On-site

Knowledge on SAS & modelling or predictive analysis Using analytical programming languages PYSpark ... This is a Contract job for you * Only US Citizen, Green Card Holder, TN Visa, GC-EAD , H4-EAD & L2 ...

MM International

Data Architect

Woodbridge, NJ · On-site

$64.25 - $82.75/hr

Woodbridge Township, NJ (Hybrid), (3 days onsite/2 wfh) Duration: 24+ Months Contract Local to NJ ... engineers • 5+ years hands-on experience working on Greenfield solutions, leading data tracks and ...

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Sas Programmer Contract information

See Springfield, NJ salary details

$15

$51

$82

How much do sas programmer contract jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for sas programmer contract in Springfield, NJ is $51.03, according to ZipRecruiter salary data. Most workers in this role earn between $35.82 and $64.09 per hour, depending on experience, location, and employer.

What are the typical responsibilities of a SAS Programmer Contract position?

As a SAS Programmer Contractor, your main responsibilities typically include developing and validating SAS code to analyze, process, and report on large datasets, often for clinical trials or business analytics. You’ll collaborate with statisticians, data managers, and project leads to ensure datasets are clean, accurate, and conform to regulatory standards. Day-to-day tasks may involve generating tables, listings, and figures, performing data QC, and documenting your programming workflow. Contractors often juggle multiple projects and must efficiently manage their time to meet strict deadlines while maintaining open communication with both internal teams and external clients.

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

To thrive as a Sas Programmer Contract, you need strong experience in SAS programming, data manipulation, statistical analysis, and a relevant degree in computer science, statistics, or a similar field. Familiarity with industry-standard tools like Base SAS, SAS/SQL, and SAS Macro, and knowledge of regulatory requirements such as CDISC, SDTM, or ADaM certifications are frequently required in clinical or data-driven roles. Excellent problem-solving, time management, and interpersonal communication skills help you adapt to dynamic project needs and collaborate with multidisciplinary teams. These skills ensure you can deliver accurate, efficient data solutions and meet project deadlines in a contract-based environment.

What is a Sas Programmer Contract job?

A SAS Programmer Contract job is a temporary or project-based role where a programmer uses SAS (Statistical Analysis System) software to manage, analyze, and report data. These professionals are often hired in industries like healthcare, finance, and clinical research to develop data-driven solutions. Contract positions may vary in length and scope, offering flexibility while requiring expertise in SAS programming, data manipulation, and statistical analysis.

What cities near Springfield, NJ are hiring for Sas Programmer Contract jobs? Cities near Springfield, NJ with the most Sas Programmer Contract job openings:
Sas Programmer Contract jobs near you
Infographic showing various Sas Programmer Contract job openings in Springfield, NJ as of June 2026, with employment types broken down into 36% Full Time, and 64% Part Time. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $106,142 per year, or $51 per hour.
Senior Manager, Biostatistics

Senior Manager, Biostatistics

Axsome Therapeutics

New York, NY • On-site

Full-time

Posted 11 days ago

Job description

Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, agitation associated with dementia due to Alzheimer's disease, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, as well as multiple novel product candidates addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X.
About This Role
Axsome Therapeutics is seeking a Senior Manager, Biostatistics to provide statistical support for multiple neurology compounds across all phases of development. Reporting to the Senior Director, Biostatistics, the Senior Manager, Biostatistics will serve as lead statistician on assigned clinical trials, and in collaboration with project team members provide statistical input on trial design, protocol development, and manage creation of Statistical Analysis Plans (SAPs). Additionally, the Senior Manager, Biostatistics will manage Contract Resource Organization (CRO) partners in the creation of statistical outputs, with hands-on quality checks of the outputs. This role will contribute to Clinical Study Report (CSR) writing, and regulatory submission documents.
This role is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles.
Job Responsibilities and Duties include, but are not limited to, the following:
  • Lead and manage all statistical activities within clinical studies (i.e. contributing to study design and selection of appropriate data analysis methods, sample size estimation)
  • Partner with other functional members, external consultants, key opinion leaders, medical advisors and CRO's/contractors, to ensure the quality and integrity of the data is maintained while identifying, and minimizing where possible, risks to the studies/projects
  • Collaborate with external CRO partners, manage creation of study SAPs based on regulatory guidance and sound statistical methodology, as well as creation of Table, Figure, and Listing shells, as per study timelines
  • Review Case Report Forms, and other supportive clinical trial documentation such as the Protocol Deviation Plan, and Data Management Plan.
  • Support clinical data reviews for data quality, outlier identification, trend analysis, and potential impact on trial results, using SAS and data visualization software, during trial conduct
  • Perform hands-on quality checks of CRO deliverables using SAS and/or R.
  • Contribute to CSR writing, including interpretation of trial results, and quality checks of data presentations.
  • Contribute to regulatory submission documents, including IND applications, FDA meeting briefing materials, and NDA submission documents, including eCRT packages.
  • Conduct ad hoc analyses using SAS and/or R in support of assigned projects.
  • Contributes to development of Standard Operating Procedures (SOPs), Work Instructions, and templates within function.
  • Ensure knowledge transfer during and at the completion of the studies/projects.
  • Stay up to date with changes in the field of statistics. Implements new ideas and advanced processes, where applicable.

Requirements / Qualifications
  • Master's degree or Ph.D. degree in Biostatistics, Statistics, Mathematics, or Medical Statistics, or a related discipline
  • At least 4 years of statistics experience with a Ph.D. degree or 7+ years with a Master's degree within the pharmaceutical industry (including contract research organizations (CROs)), biotechnology or medical sector, including clinical trial design, analysis and reporting
  • Experience in Phase III and III pivotal clinical development studies
  • Strong statistical programming skills in SAS
  • Ability to work on-site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles

Experience, Knowledge and Skills
  • Modeling and simulation skills are preferred
  • Strong ability to manage time and resources, ensuring the successful achievement of pre-determined deadlines
  • Flexibility in approach, while ensuring the delivery of high-quality work in a dynamic work environment, with competing priorities
  • Experience marketing application submissions to regulatory authorities is strongly preferred
  • Experience overseeing and managing CRO's statistical analysis of assigned clinical trials
  • Excellent communication and presentation skills (written and verbal)
  • Demonstrated ability to effectively interact with internal team members and external parties that do not possess the knowledge and background to readily understand the application of statistics to drug development and study outcomes

Salary & Benefits
The anticipated salary range for this role is $140,000-$170,000. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package.
Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law.
Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.

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