cGxPServe
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SAS Programmer
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cGxPServe 1 day ago Be among the first 25 applicants Join to apply for the
SAS Programmer
role at
cGxPServe Get AI-powered advice on this job and more exclusive features. Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications) Programs quality checks for clinical study raw data and report the findings to Data Management Provides input in the design and development of case report forms and clinical study databases. Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Provides programming support for adhoc analysis.
Responsibilities
Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications) Programs quality checks for clinical study raw data and report the findings to Data Management Provides input in the design and development of case report forms and clinical study databases. Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Provides programming support for adhoc analysis.
Requirements
MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 4+ years. Experience in providing statistical programming support to early and late phase clinical trials. Excellent skills in SAS programming and statistical reporting. Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements. Familiarity with FDA and ICH regulations and guidelines. Excellent problem-solving skills. Good written and verbal communication skills and organizational and documentation skills. Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Information Technology Industries
Research Services Referrals increase your chances of interviewing at cGxPServe by 2x Sign in to set job alerts for SAS Developer roles.
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SAS Programmer
role at
cGxPServe 1 day ago Be among the first 25 applicants Join to apply for the
SAS Programmer
role at
cGxPServe Get AI-powered advice on this job and more exclusive features. Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications) Programs quality checks for clinical study raw data and report the findings to Data Management Provides input in the design and development of case report forms and clinical study databases. Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Provides programming support for adhoc analysis.
Responsibilities
Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications) Programs quality checks for clinical study raw data and report the findings to Data Management Provides input in the design and development of case report forms and clinical study databases. Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Provides programming support for adhoc analysis.
Requirements
MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 4+ years. Experience in providing statistical programming support to early and late phase clinical trials. Excellent skills in SAS programming and statistical reporting. Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements. Familiarity with FDA and ICH regulations and guidelines. Excellent problem-solving skills. Good written and verbal communication skills and organizational and documentation skills. Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Information Technology Industries
Research Services Referrals increase your chances of interviewing at cGxPServe by 2x Sign in to set job alerts for SAS Developer roles.
New York, NY $99,900.00-$133,900.00 1 day ago New York, NY $90,000.00-$115,000.00 16 hours ago New York, NY $129,000.00-$135,000.00 2 weeks ago Data Analyst- $150,000-$200,000 + bonus!
New York City Metropolitan Area $150,000.00-$200,000.00 1 week ago New York, NY $124,000.00-$176,000.00 1 week ago New York, NY $62,000.00-$102,300.00 1 day ago Manhattan, NY $90,000.00-$130,000.00 2 months ago New York, NY $120,000.00-$150,000.00 2 weeks ago New York City Metropolitan Area $50.00-$60.00 4 weeks ago 2025 Internship, Fall - Data Science (Remote)
New York, NY $60,000.00-$70,000.00 10 hours ago New York, NY $106,000.00-$133,000.00 2 weeks ago Data Analyst - (ACE), Emerging Talent Intern
New York, NY $79,200.00-$96,800.00 3 weeks ago New York, NY $90,000.00-$110,000.00 1 day ago New York, NY $140,000.00-$170,000.00 4 weeks ago Whippany, NJ $150,550.00-$165,605.00 2 weeks ago New York, NY $85,600.00-$112,000.00 1 day ago New York City Metropolitan Area $80,000.00-$90,000.00 1 week ago Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr