Katalyst CRO
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Clinical SAS Programmer
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Katalyst CRO 2 days ago Be among the first 25 applicants Join to apply for the
Clinical SAS Programmer
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). 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. Programs for 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 aCRF, SDTM and ADaM datasets specifications for datasets programming.
Responsibilities
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). 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. Programs for 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 aCRF, SDTM and ADaM datasets specifications for datasets programming.
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 5 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. Ability to prioritize and multi-task effectively. Demonstrated positive attitude and the ability to work well with others. Seniority level
Seniority level
Associate Employment type
Employment type
Contract Job function
Job function
Information Technology Industries
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Clinical SAS Programmer
role at
Katalyst CRO 2 days ago Be among the first 25 applicants Join to apply for the
Clinical SAS Programmer
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). 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. Programs for 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 aCRF, SDTM and ADaM datasets specifications for datasets programming.
Responsibilities
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). 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. Programs for 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 aCRF, SDTM and ADaM datasets specifications for datasets programming.
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 5 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. Ability to prioritize and multi-task effectively. Demonstrated positive attitude and the ability to work well with others. Seniority level
Seniority level
Associate Employment type
Employment type
Contract Job function
Job function
Information Technology Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new SAS Developer jobs in
Newark, NJ . New York, NY $220,000.00-$260,000.00 4 days ago New York, NY $70,000.00-$150,000.00 1 week ago Brooklyn, NY $150,000.00-$200,000.00 3 months ago New York, NY $130,000.00-$180,000.00 6 months ago New York, NY $99,500.00-$200,000.00 1 day ago New York, NY $140,000.00-$200,000.00 1 week ago New York, NY $120,000.00-$180,000.00 5 months ago Full Stack Software Engineer (All Levels)
Want to work with us, but don't see the right job listed?
New York, NY $163,200.00-$223,200.00 1 week ago New York, NY $140,000.00-$140,000.00 1 month ago New York, NY $110,000.00-$150,000.00 1 month ago New York, NY $99,500.00-$200,000.00 1 day ago New York, NY $70,000.00-$150,000.00 2 days ago New York, NY $235,000.00-$255,000.00 1 week ago New York, NY $120,000.00-$140,000.00 2 weeks ago New York, NY $140,000.00-$170,000.00 2 months ago New York, NY $145,000.00-$260,000.00 8 months ago Backend Software Engineer, CloudKitchens - New York City
New York, NY $140,000.00-$200,000.00 1 month ago New York, NY $165,000.00-$165,000.00 1 year ago New York, NY $141,000.00-$202,000.00 3 days ago New York, NY $120,000.00-$220,000.00 1 month ago Backend Engineer, Real-time supply management
New York, NY $128,000.00-$160,000.00 2 weeks ago Software Engineer - Frontend / Fullstack
New York, NY $140,000.00-$200,000.00 1 month ago New York, NY $100,500.00-$173,250.00 1 month ago New York, NY $140,000.00-$230,000.00 3 months ago New York, NY $100,000.00-$200,000.00 6 months ago Don't see the right opportunity? Apply here!
New York, NY $140,000.00-$185,000.00 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