Katalyst CRO
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SAS Programmer
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Katalyst CRO 1 day ago Be among the first 25 applicants Join to apply for the
SAS Programmer
role at
Katalyst CRO 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
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SAS Programmer
role at
Katalyst CRO 1 day ago Be among the first 25 applicants Join to apply for the
SAS Programmer
role at
Katalyst CRO 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
Biotechnology Research and IT Services and IT Consulting Referrals increase your chances of interviewing at Katalyst CRO by 2x Sign in to set job alerts for SAS Developer roles.
Manhattan, NY $90,000.00-$130,000.00 2 months ago Manhattan, NY $79,473.00-$91,394.00 1 week ago New York County, NY $180,000.00-$200,000.00 1 month ago Data Analyst Cycling & Micromobility Unit
Capgemini Invent, Customer-Centric Data Analytics - Senior Consultant
New York County, NY $120,000.00-$150,000.00 3 weeks ago Manhattan, NY $87,743.00-$100,904.00 1 month ago Manhattan, NY $84,087.00-$90,680.00 7 months ago Capgemini Invent, Customer Analytics Sr. Consultant
New York County, NY $120,000.00-$150,000.00 1 month ago Manhattan, NY $104,550.00-$172,200.00 5 days ago Senior Data Analyst, Bureau of Vital Statistics
Assistant Director, Systems and Data Analysis, SIPR (OM/WBE)
Manhattan, NY $52,791.00-$60,710.00 6 months 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