Senior Statistical Programmer
Rahway, NJ · On-site
Significant SAS or R programming experience for data manipulation, analysis and reporting * Designs ... Implements statistical methods not currently available through commercial software packages
Rahway, NJ · On-site
Significant SAS or R programming experience for data manipulation, analysis and reporting * Designs ... Implements statistical methods not currently available through commercial software packages
Rahway, NJ · On-site
Significant SAS or R programming experience for data manipulation, analysis and reporting * Designs ... Implements statistical methods not currently available through commercial software packages
Experience in CDISC SDTM and ADaM standardsSignificant SAS or R programming experience for data ... Implements statistical methods not currently available through commercial software ...
Experience in CDISC SDTM and ADaM standardsSignificant SAS or R programming experience for data ... Implements statistical methods not currently available through commercial software ...
Jersey City, NJ · On-site
The role of the Senior Statistical Programmer is to perform statistical programming activities for ... with SAS in a pharmaceutical or CRO environment Bachelor's Degree or above in Statistics ...
Jersey City, NJ · On-site
The role of the Senior Statistical Programmer is to perform statistical programming activities for ... with SAS in a pharmaceutical or CRO environment Bachelor's Degree or above in Statistics ...
East Hanover, NJ · On-site
Knowledge of other data review/statistics software packages like Jreview ... SAS software systems experience. Experience in research programming preferred. Knowledge about ...
East Hanover, NJ · On-site
Knowledge of other data review/statistics software packages like Jreview ... SAS software systems experience. Experience in research programming preferred. Knowledge about ...
... programming ... BASE SAS cert * Expert knowledge of base SAS and SAS Macros for SAS software development * Design ...
... programming ... BASE SAS cert * Expert knowledge of base SAS and SAS Macros for SAS software development * Design ...
Newark, NJ · On-site
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.
Newark, NJ · On-site
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics ...
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics ...
East Brunswick, NJ · On-site +1
... programming ... BASE SAS cert * Expert knowledge of base SAS and SAS Macros for SAS software development * Design ...
East Brunswick, NJ · On-site +1
... programming ... BASE SAS cert * Expert knowledge of base SAS and SAS Macros for SAS software development * Design ...
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics ...
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics ...
Candidate to provide statistical programming support and validation and help set specifications of ... Intermediate Pharma industry SAS experience required, with 2-5 year s experience in a medical ...
Candidate to provide statistical programming support and validation and help set specifications of ... Intermediate Pharma industry SAS experience required, with 2-5 year s experience in a medical ...
Franklin Lakes, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Franklin Lakes, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Franklin Lakes, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Franklin Lakes, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Morristown, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Morristown, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Branchburg, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Branchburg, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Totowa, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Totowa, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Bridgewater, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Bridgewater, NJ · On-site +1
Ability to program, document, and validate statistical software code in at least one statistical programming language, such as R or SAS, is required. * 3+ years of experience of relevant experience ...
Bridgewater, NJ · On-site +1
$112K - $175K/yr
Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in ...
Bridgewater, NJ · On-site +1
$112K - $175K/yr
Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in ...
Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming ...
Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming ...
Bridgewater, NJ · On-site +1
$112K - $175K/yr
Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in ...
Bridgewater, NJ · On-site +1
$112K - $175K/yr
Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in ...
Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming ...
Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming ...
$5.79 - $13.91
0% of jobs
$13.91 - $22.04
0% of jobs
$27.58 is the 25th percentile. Wages below this are outliers.
$22.04 - $30.17
37% of jobs
$30.17 - $38.30
0% of jobs
$38.30 - $46.43
0% of jobs
$46.43 - $54.56
0% of jobs
$54.56 - $62.69
6% of jobs
The median wage is $67.86 / hr.
$62.69 - $70.82
11% of jobs
$70.82 - $78.94
11% of jobs
$78.94 - $87.07
7% of jobs
$87.83 is the 75th percentile. Wages above this are outliers.
$87.07 - $95.20
28% of jobs
$5
$62
$95
Sas Statistical Programmers often work on projects involving the analysis and reporting of clinical trial or observational study data, producing datasets, tables, listings, and figures to support regulatory submissions or scientific publications. They routinely collaborate with biostatisticians, clinical data managers, and project managers to ensure data quality and compliance with industry standards. Daily responsibilities include coding in SAS, validating datasets, troubleshooting data issues, and preparing documentation. Effective communication and teamwork are essential, as the role frequently involves working in multidisciplinary teams to meet project goals and timelines.
A SAS Statistical Programmer is a professional who utilizes SAS software to manage, analyze, and report statistical data, primarily in industries like pharmaceuticals, healthcare, and clinical research. They write and validate programs to generate tables, listings, and figures for clinical trials or other data-driven studies. Their role involves ensuring data accuracy, compliance with regulatory guidelines, and collaboration with statisticians and researchers to support decision-making.
To thrive as a Sas Statistical Programmer, you need a strong background in statistics, programming (especially SAS), and data management, usually supported by a degree in statistics, computer science, or a related field. Familiarity with SAS Base, SAS Macro, and clinical data standards like CDISC, as well as relevant industry certifications, are commonly required. Attention to detail, strong problem-solving abilities, and effective communication skills are valuable soft skills. These competencies ensure accurate data analysis, clear reporting, and successful collaboration within cross-functional teams in fields like healthcare or pharmaceuticals.

Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 2 days ago
Job Description
Responsibilities:
This position provides high quality statistical programming deliverables for global stakeholders in Early Development Statistics and/or PK/PD Modeling and Simulation spanning all our Company's therapeutic areas. The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables, listings and figures according to statistical/modeling analysis plan. The senior programmer will partner with stakeholders to solve problems; reduce the amount of programming tasks being completed by stakeholders to facilitate an increase in efficiency and compliance for the analyses. The senior programmer will also write programs to analyze data with statistical methods which are not currently available through commercial software packages. The programmer will be a key collaborator with statisticians, pharmacokinetic (PK) modelers, and other project stakeholders.
Primary Activities:
Programmatically develop, validate and maintain complex datasets, tables, listings, and figures
Provide technical consultation and analytical support to statisticians and PK modelers for exploratory and unplanned statistical analyses
Prepare compliant programming code for regulatory submissions including analysis datasets, tables, listings, figures and associated documentation
Ensure programmatic traceability from data source to analysis / modeling result
Support the development of programming standards to enable efficient and high quality production of programming deliverables
Education and Minimum Requirement:
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS/R programming experience in a clinical trial environment
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS/R 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 research and development projects (data, analyses, tables, graphics, listings)
A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders
Specific Required Skills and Experience:
Experience in CDISC SDTM and ADaM standards
Significant SAS or R programming experience for data manipulation, analysis and reporting
Designs and develops complex programming algorithms
Ability to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packages
Demonstrated ability to work in an exploratory environment, handling non-standard data in a variety of formats with minimal requirements; knowledge of pharmaceutical development processes
Preferred Skills and Experience:
Programming expertise with pharmacokinetic data (raw concentration data, derived PK parameters)
Familiarity with clinical pharmacology concepts and pharmacokinetics concepts
Efficiently manipulates very large databases including complex data preprocessing, filtering, and manipulation; programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters)
Experience with at least one other software than SAS (e.g., R, Python, NonMem)
Good working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)
Utilizes and contributes to the development of standard departmental SAS macros
Ability and interest to work across cultures and geographies
Ability to complete statistical programming deliverables through the use of global outsource partner programming staff
Active in professional societies
BARDS2020
eligibleforERP
SPjobs
VETJOBS
EBRG
Required Skills:
Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical ProgrammingPreferred Skills:
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The 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:
RegularRelocation:
DomesticVISA Sponsorship:
YesTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
08/19/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.