SAS Programmer
East Brunswick, NJ · On-site
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
East Brunswick, NJ · On-site
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
East Brunswick, NJ · On-site
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
East Brunswick, NJ · On-site +1
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
East Brunswick, NJ · On-site +1
Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming. Additional Information Visa Status * Only US Citizens, Green Card, EAD and OPT holders. * No H1B ...
Madison, NJ · On-site
Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR); Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets ...
Madison, NJ · On-site
Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR); Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets ...
* Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... Expert knowledge of/experience with SAS software. * Good understanding of global clinical trials ...
* Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... Expert knowledge of/experience with SAS software. * Good understanding of global clinical trials ...
East Brunswick, NJ · On-site +1
Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... Expert knowledge of/experience with SAS software. * Good understanding of global clinical trials ...
East Brunswick, NJ · On-site +1
Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming ... Expert knowledge of/experience with SAS software. * Good understanding of global clinical trials ...
Parsippany Troy Hills, NJ · On-site
$120 - $160/hr
... based clinical development, involving statistical planning, analysis, and reporting for clinical studies. The ideal candidate will have a strong background in statistics and SAS programming ...
Parsippany Troy Hills, NJ · On-site
$120 - $160/hr
... based clinical development, involving statistical planning, analysis, and reporting for clinical studies. The ideal candidate will have a strong background in statistics and SAS programming ...
... clinical trials. The work include mainly performing data review and statistical analysis ... The candidate should be proficient in SAS programming (eg., Data steps, PROC ANCOVA, PROC MIXED ...
... clinical trials. The work include mainly performing data review and statistical analysis ... The candidate should be proficient in SAS programming (eg., Data steps, PROC ANCOVA, PROC MIXED ...
Raritan, NJ · On-site
Biostatistician / Clinical Data Detailed Description: * Responsible for statistical aspects of ... Work with SAS programmers as part of a biostatistics team. * Knowledge of applied parametric and ...
Raritan, NJ · On-site
Biostatistician / Clinical Data Detailed Description: * Responsible for statistical aspects of ... Work with SAS programmers as part of a biostatistics team. * Knowledge of applied parametric and ...
... clinical trials, or other sources as per provided specifications Conduct analytic quality assurance procedures and ensure quality of final deliveries Develop SAS macro libraries to standardize ...
... clinical trials, or other sources as per provided specifications Conduct analytic quality assurance procedures and ensure quality of final deliveries Develop SAS macro libraries to standardize ...
East Hanover, NJ · On-site
SAS software systems experience. Experience in research programming preferred. Knowledge about clinical trials a plus. Ability to perform effectively in team environment and good communications ...
East Hanover, NJ · On-site
SAS software systems experience. Experience in research programming preferred. Knowledge about clinical trials a plus. Ability to perform effectively in team environment and good communications ...
Raritan, NJ · On-site
SAS Programming; Clinical data management; Clinical Trials Management; Regulatory Affairs; Clinical Communications; Clinical Pharmacology; Medical Writing, Quality Management 3. Contacts Outside the ...
Raritan, NJ · On-site
SAS Programming; Clinical data management; Clinical Trials Management; Regulatory Affairs; Clinical Communications; Clinical Pharmacology; Medical Writing, Quality Management 3. Contacts Outside the ...
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Brooklyn, NY · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Brooklyn, NY · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Montclair, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Montclair, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Clifton, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Clifton, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Weehawken, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Weehawken, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Union City, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Union City, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Bayonne, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Bayonne, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Maplewood, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Maplewood, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Kearny, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
Kearny, NJ · On-site
We are seeking a Senior Statistical Analyst with strong expertise in SAS and R programming, CDISC standards, and clinical trial data analysis. The ideal candidate will collaborate with statisticians ...
$19.49 - $25.12
4% of jobs
$25.12 - $30.75
9% of jobs
$30.75 - $36.37
4% of jobs
$36.37 - $42
7% of jobs
$42.35 is the 25th percentile. Wages below this are outliers.
$42 - $47.63
9% of jobs
The median wage is $53.25 / hr.
$47.63 - $53.25
17% of jobs
$53.25 - $58.88
7% of jobs
$58.88 - $64.51
14% of jobs
$66.30 is the 75th percentile. Wages above this are outliers.
$64.51 - $70.13
12% of jobs
$70.13 - $75.76
10% of jobs
$75.76 - $81.38
7% of jobs
$19
$54
$81
An Entry Level Clinical SAS Programmer is responsible for programming and analyzing clinical trial data using SAS software. They assist in creating datasets, reports, and statistical outputs that comply with regulatory standards. Their work supports biostatisticians and clinical teams in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role requires knowledge of SAS programming, clinical research processes, and regulatory requirements such as CDISC standards. It is an excellent starting point for those looking to build a career in clinical data analysis and biostatistics.
Entry Level Clinical SAS Programmers are primarily responsible for writing and validating SAS code to process clinical trial data, generate tables, listings, and figures, and support statistical analysis plans. They work closely with biostatisticians, data managers, and other team members to ensure data integrity and compliance with regulatory standards. Daily tasks may involve data cleaning, programming data checks, and documenting code for reproducibility. This role offers great exposure to the clinical data lifecycle and provides a strong foundation for professional growth within clinical research and data analytics.
To thrive as an Entry Level Clinical SAS Programmer, you need a solid understanding of SAS programming, statistics, and clinical trial processes, often supported by a degree in computer science, statistics, or a related field. Familiarity with SAS software, data management systems, and FDA or CDISC standards is highly valued, and SAS certification can be a plus. Attention to detail, strong problem-solving skills, and effective communication are key soft skills for this role. These competencies ensure high-quality data analysis, regulatory compliance, and clear collaboration across teams in pharmaceutical or clinical research settings.
The most popular types of Clinical Sas Programmer jobs in Edison, NJ are:
The top searched job categories for Entry Level Clinical Sas Programmer jobs in Edison, NJ are:
Cities near Edison, NJ with the most Entry Level Clinical Sas Programmer job openings:

Visa Status
Sourced by ZipRecruiter
51 - 200 Employees
Camarillo, CA, US
1979