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Sas Clinical Data Jobs (NOW HIRING)

SAS Programmer

Fort Detrick, MD · On-site

$135K - $148K/yr

Collaborate with Clinical Data Management and Biostatistics teams. * Maintain programming ... SAS Advanced Programmer Certification required. * Minimum 7 years of clinical SAS programming ...

SAS Programmer

Fort Detrick, MD · On-site

$135K - $148K/yr

Collaborate with Clinical Data Management and Biostatistics teams. * Maintain programming ... SAS Advanced Programmer Certification required. * Minimum 7 years of clinical SAS programming ...

SAS Certified Platform Administrator or SAS Certified Deployment Specialist credential ... As an experienced Clinical Data AMS Senior Consultant you will have the ability to share new ideas ...

SAS Certified Platform Administrator or SAS Certified Deployment Specialist credential ... As an experienced Clinical Data AMS Senior Consultant you will have the ability to share new ideas ...

SAS Certified Platform Administrator or SAS Certified Deployment Specialist credential ... As an experienced Clinical Data AMS Senior Consultant you will have the ability to share new ideas ...

SAS Certified Platform Administrator or SAS Certified Deployment Specialist credential ... As an experienced Clinical Data AMS Senior Consultant you will have the ability to share new ideas ...

Showing results 41-60

Sas Clinical Data information

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$19

$54

$80

How much do sas clinical data jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for sas clinical data in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What is a SAS Clinical Data professional?

SAS Clinical Data professionals are experts who use SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and healthcare industries. They play a key role in ensuring the accuracy, integrity, and regulatory compliance of clinical data. Their work involves data cleaning, manipulation, statistical analysis, and the preparation of reports for regulatory submissions. These professionals often collaborate with clinical researchers, statisticians, and regulatory teams to support drug development and approval processes.

What are the key skills and qualifications needed to thrive as a SAS Clinical Data analyst?

To thrive as a SAS Clinical Data Analyst, you need a solid background in statistics, data management, and clinical research, typically supported by a degree in life sciences, statistics, or a related field. Proficiency in SAS programming, knowledge of CDISC standards (SDTM/ADaM), and familiarity with clinical trial data systems such as EDC are essential. Strong attention to detail, problem-solving abilities, and effective communication skills set outstanding analysts apart. These competencies ensure accurate data analysis, regulatory compliance, and clear reporting, all critical for successful clinical trials.

What are some common challenges faced by SAS Clinical Data professionals when working with large clinical trial datasets?

SAS Clinical Data professionals often encounter challenges such as handling missing or inconsistent data, ensuring data integrity, and adhering to strict regulatory requirements. Managing large and complex datasets requires strong attention to detail and effective communication with clinical research teams to clarify data discrepancies. Additionally, tight project deadlines and evolving study protocols can make prioritizing tasks and maintaining high data quality demanding. Collaborating closely with biostatisticians and data managers is essential for successful data cleaning, validation, and analysis.

What is the difference between Sas Clinical Data vs Clinical Data Analyst?

AspectSas Clinical DataClinical Data Analyst
Required CredentialsExperience with SAS, biostatistics, clinical research certificationsDegree in life sciences, data analysis skills, some SAS knowledge
Work EnvironmentPharmaceutical companies, CROs, clinical research settingsHealthcare organizations, research institutions, biotech firms
Employer & Industry UsagePrimarily in clinical trial data managementBroader data analysis in healthcare and research

While both roles involve handling clinical data, Sas Clinical Data specialists focus on managing and analyzing clinical trial data using SAS software, often requiring specific certifications. Clinical Data Analysts may work across various healthcare settings, utilizing a broader range of data tools. Understanding these differences helps in choosing the right career path or job search focus.

More about Sas Clinical Data jobs
Infographic showing various Sas Clinical Data job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

SAS Programmer

VENESCO, LLC

Fort Detrick, MD • On-site

$135K - $148K/yr

Full-time

Re-posted 10 days ago


Job description

Description

SAS Programmer


Venesco is seeking skilled SAS Programmers to develop validated statistical programs and CDISC-compliant datasets to support clinical trials, statistical analyses, safety reporting, and FDA submissions.   


Requirements

 Duties and Responsibilities 

  • Develop and validate SAS programs. 
  • Produce Tables, Listings, and Figures (TLFs). 
  • Generate SDTM, ADaM, and SEND datasets. 
  • Develop define.xml files and reviewer guides. 
  • Create programming validation plans and reports. 
  • Develop randomization programs and statistical outputs. 
  • Support interim and final analyses. 
  • Assist with FDA submission packages. 
  • Collaborate with Clinical Data Management and Biostatistics teams. 
  • Maintain programming documentation and standards. 

Minimum Qualifications 

  • Bachelor's degree in Statistics, Computer Science, Mathematics, or related field. 
  • SAS Advanced Programmer Certification required. 
  • Minimum 7 years of clinical SAS programming experience. 
  • Extensive experience with CDISC, SDTM, and ADaM standards. 
  • Experience supporting FDA submissions. 
  • Strong knowledge of validation practices and regulatory requirements  

Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit https://venesco.com.