Job Title: SAS Programmer II / Clinical Trials / Remote Work Duration: 21 months contract ... Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development ...
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Job Title: SAS Programmer II / Clinical Trials / Remote Work Duration: 21 months contract ... Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development ...
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New
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Position Overview We are seeking a Senior SAS SQL Developer with strong expertise in SAS ... Advanced SQL skills with experience working on large datasets. * Strong understanding of data ...
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Position Overview We are seeking a Senior SAS SQL Developer with strong expertise in SAS ... Advanced SQL skills with experience working on large datasets. * Strong understanding of data ...
Sas Advanced Programmer information
See salary details
$14.66 - $20.56
4% of jobs
$20.56 - $26.46
2% of jobs
$26.46 - $32.36
15% of jobs
$34.38 is the 25th percentile. Wages below this are outliers.
$32.36 - $38.26
12% of jobs
$38.26 - $44.17
14% of jobs
The median wage is $45.64 / hr.
$44.17 - $50.07
15% of jobs
$50.07 - $55.97
11% of jobs
$58.36 is the 75th percentile. Wages above this are outliers.
$55.97 - $61.87
8% of jobs
$61.87 - $67.77
9% of jobs
$67.77 - $73.67
3% of jobs
$73.67 - $79.57
7% of jobs
$14
$49
$79
How much do sas advanced programmer jobs pay per hour?
As of Aug 19, 2026, the average hourly pay for sas advanced programmer 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 Advanced Programmer?
SAS Advanced Programmers are professionals who use advanced features of the SAS software suite to manage, analyze, and report on large sets of data. They are skilled in writing complex SAS programs, including macros and advanced SQL, and are proficient in data manipulation, statistical analysis, and automating tasks. These programmers often work in fields like healthcare, finance, and research, helping organizations extract actionable insights from data. They may also prepare data for statistical modeling or reporting purposes and often hold certifications such as SAS Certified Advanced Programmer.
What are the key skills and qualifications needed to thrive as a SAS Advanced Programmer?
To thrive as a SAS Advanced Programmer, you need advanced knowledge of SAS programming, data manipulation, and statistical analysis, often supported by a bachelor's degree in a quantitative field and SAS certifications. Expertise in using tools like SAS Base, SAS Macro, and Enterprise Guide, along with familiarity with databases and data warehousing systems, is typically required. Strong problem-solving skills, attention to detail, and effective communication help you collaborate with teams and interpret complex data. These skills are crucial for delivering accurate data insights and supporting robust business or research decisions.
What are some typical challenges faced by SAS Advanced Programmers when working on large-scale data projects?
SAS Advanced Programmers often encounter challenges such as optimizing code for performance when handling massive datasets, ensuring data integrity across complex transformations, and managing resource constraints in shared computing environments. Collaborating with data analysts, statisticians, and IT teams to align on data requirements and troubleshooting unexpected results are also common. Being proactive in documenting code and maintaining clear communication helps overcome these challenges and ensures project success.
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What job categories do people searching Sas Advanced Programmer jobs look for?
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Contractor
Re-posted 29 days ago
Job description
Position Details:
Our client, a world-leading Pharmaceutical Company in Memphis, TN is currently looking for a SAS Programmer II to join their expanding team.
Job Title: SAS Programmer II / Clinical Trials / Remote Work
Duration: 21 months contract, extendable up to 24 Months
Location: Remote Worker
Our client, a world-leading Pharmaceutical Company in Memphis, TN is currently looking for a SAS Programmer II to join their expanding team.
Job Title: SAS Programmer II / Clinical Trials / Remote Work
Duration: 21 months contract, extendable up to 24 Months
Location: Remote Worker
Client Location: Memphis, TN
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Title: Clinical Programming – Contractor – Analysis and Reporting (ADaM)
Shift Schedule:
Shift Schedule:
Regular 40 week working schedule (morning)
Duration:
Duration:
Up to 2 year assignment
Temp to Perm:
Temp to Perm:
Not during this time
Core Essential Skill Sets:
1. Bachelors + 5 year, Masters + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer
2. Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
Position Summary:
The Clinical Programming (Contractor) is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials.
The clinical programming contractor independently manages completed projects that involve global tasks, or cross functional teams
Core Essential Skill Sets:
1. Bachelors + 5 year, Masters + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer
2. Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
Position Summary:
The Clinical Programming (Contractor) is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials.
The clinical programming contractor independently manages completed projects that involve global tasks, or cross functional teams
The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing programming support for publication for our marketed drugs.
Travel Requirements:
Travel Requirements:
N/A
Essential Duties & Responsibilities:
1. Primarily works at the Study, product / program level
2. Provides comprehensive programming support, including development of programs, ADaM specifications, analysis (datasets, TLFs) complying with regulatory requirements, departmental SOPs and work practices.
3. Manages and Delivers assignments with good quality and within timelines
4. Provides programming support to CDISC based e-submission. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets and TLFs.
5. Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource gaps.
6. Responsible for the standardization of GSD deliverables (TLGs, Datasets) across study projects within an indication/therapeutic area. Provides input on opportunities for process improvement
7. Proactively communicates issues impacting programming deliverables with Stat or DM team members.
Position Requirements:
Education Required:
Essential Duties & Responsibilities:
1. Primarily works at the Study, product / program level
2. Provides comprehensive programming support, including development of programs, ADaM specifications, analysis (datasets, TLFs) complying with regulatory requirements, departmental SOPs and work practices.
3. Manages and Delivers assignments with good quality and within timelines
4. Provides programming support to CDISC based e-submission. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets and TLFs.
5. Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource gaps.
6. Responsible for the standardization of GSD deliverables (TLGs, Datasets) across study projects within an indication/therapeutic area. Provides input on opportunities for process improvement
7. Proactively communicates issues impacting programming deliverables with Stat or DM team members.
Position Requirements:
Education Required:
Bachelor’s Degree/Master’s Degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
Experience Required:
Bachelors + 5 year, Masters + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer.
Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
Strong understanding of SDTM, ADaM standards and Implementation guides.
Demonstrated proficiency in using SAS to produce analysis datasets, TLFs, eSUB components and using other software applications (eg. Pinnacle 21, XML and MS Office)
Demonstrated ability to work independently and in a team environment.
Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
Strong understanding of SDTM, ADaM standards and Implementation guides.
Demonstrated proficiency in using SAS to produce analysis datasets, TLFs, eSUB components and using other software applications (eg. Pinnacle 21, XML and MS Office)
Demonstrated ability to work independently and in a team environment.
Experience Preferred:
Specialized or Technical Knowledge Licenses, Certifications needed:
Functional Knowledge: Expert level of programming skills and problem resolution in SAS.
Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated TLGs in study/project (e.g. ISS/ISE), creation of Bioresearch Monitoring (BIMO) Inspections).
Have solid knowledge of statistical models used for efficacy data analysis.
Company/Industry Related Knowledge: Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development in multiple therapeutic areas.
Job-Specific Competencies:
1. Tackles difficult problems; identifies solutions and recommends action management
2. Influences communication toward common understanding and actionable results;
3. Good oral and written communication skills.
Specialized or Technical Knowledge Licenses, Certifications needed:
Functional Knowledge: Expert level of programming skills and problem resolution in SAS.
Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated TLGs in study/project (e.g. ISS/ISE), creation of Bioresearch Monitoring (BIMO) Inspections).
Have solid knowledge of statistical models used for efficacy data analysis.
Company/Industry Related Knowledge: Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development in multiple therapeutic areas.
Job-Specific Competencies:
1. Tackles difficult problems; identifies solutions and recommends action management
2. Influences communication toward common understanding and actionable results;
3. Good oral and written communication skills.