Katalyst CRO
Statistical Analyst
Katalyst CRO - Miami, Florida, us, 33222
Work at Katalyst CRO
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Overview
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Statistical Analyst
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Katalyst CRO 1 day ago Be among the first 25 applicants Join to apply for the
Statistical Analyst
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Katalyst CRO Get AI-powered advice on this job and more exclusive features. Leads the statistical programming activities for projects with lower complexity. Leads the statistical programming activities for studies. Develop SAS programs for the creation of Adam data sets following CDISC standards. Develop SAS programs for the creation of Tables, Listings and Figures. Validation of Adam data sets, Tables, Listings and Figures. Create specifications for the structure of Adam data sets for individual studies and integrated data. Create documentation for regulatory filings including reviewers' guides and data definition documents. Leads the development of standard SAS Macros and participates in the development of standard operating procedures. Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
Responsibilities
Leads the statistical programming activities for projects with lower complexity. Leads the statistical programming activities for studies. Develop SAS programs for the creation of Adam data sets following CDISC standards. Develop SAS programs for the creation of Tables, Listings and Figures. Validation of Adam data sets, Tables, Listings and Figures. Create specifications for the structure of Adam data sets for individual studies and integrated data. Create documentation for regulatory filings including reviewers' guides and data definition documents. Leads the development of standard SAS Macros and participates in the development of standard operating procedures. Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
Requirements:
MS in Statistics, Computer Science or a related field with 6+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience. In depth understanding of SAS programming concepts and techniques related to drug development. Fundamental understanding of CDISC Standards. Fundamental understanding of the drug development process, including experience with regulatory filings. Ability to communicate clearly both oral and written. Ability to accurately estimate effort required for study related programming activities. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
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Statistical Analyst
role at
Katalyst CRO 1 day ago Be among the first 25 applicants Join to apply for the
Statistical Analyst
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. Leads the statistical programming activities for projects with lower complexity. Leads the statistical programming activities for studies. Develop SAS programs for the creation of Adam data sets following CDISC standards. Develop SAS programs for the creation of Tables, Listings and Figures. Validation of Adam data sets, Tables, Listings and Figures. Create specifications for the structure of Adam data sets for individual studies and integrated data. Create documentation for regulatory filings including reviewers' guides and data definition documents. Leads the development of standard SAS Macros and participates in the development of standard operating procedures. Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
Responsibilities
Leads the statistical programming activities for projects with lower complexity. Leads the statistical programming activities for studies. Develop SAS programs for the creation of Adam data sets following CDISC standards. Develop SAS programs for the creation of Tables, Listings and Figures. Validation of Adam data sets, Tables, Listings and Figures. Create specifications for the structure of Adam data sets for individual studies and integrated data. Create documentation for regulatory filings including reviewers' guides and data definition documents. Leads the development of standard SAS Macros and participates in the development of standard operating procedures. Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
Requirements:
MS in Statistics, Computer Science or a related field with 6+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience. In depth understanding of SAS programming concepts and techniques related to drug development. Fundamental understanding of CDISC Standards. Fundamental understanding of the drug development process, including experience with regulatory filings. Ability to communicate clearly both oral and written. Ability to accurately estimate effort required for study related programming activities. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
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