Katalyst CRO
Overview
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Sr. Statistical Analyst
role at
Katalyst CRO .
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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.
Lead the development of standard SAS Macros and participate in the development of standard operating procedures.
Provide 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 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 orally and in writing.
Ability to accurately estimate effort required for study related programming activities.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Sr. Statistical Analyst
role at
Katalyst CRO .
Get AI-powered advice on this job and more exclusive features.
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.
Lead the development of standard SAS Macros and participate in the development of standard operating procedures.
Provide 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 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 orally and in writing.
Ability to accurately estimate effort required for study related programming activities.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr