

SAS Analyst
β - Featured Role | Apply direct with Data Freelance Hub
This role is for a SAS Analyst with a contract length of "unknown" and a pay rate of "unknown." Required skills include SAS programming, CDISC standards, and drug development experience. A Master's degree with 6+ years or a Bachelor's with 8+ years is needed.
π - Country
United States
π± - Currency
$ USD
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π° - Day rate
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ποΈ - Date discovered
July 9, 2025
π - Project duration
Unknown
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ποΈ - Location type
Unknown
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π - Contract type
Unknown
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π - Security clearance
Unknown
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π - Location detailed
Los Angeles, CA
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π§ - Skills detailed
#Documentation #CDISC (Clinical Data Interchange Standards Consortium) #Macros #ADaM (Analysis Data Model) #Computer Science #Data Science #SAS #Statistics #Programming
Role description
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Company Description
β’ Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
β’ We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description
Job Description:
β’ The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products.
β’ The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity.
β’ The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations.
Responsibilities:
β’ Leads the statistical programming activities for projects with lower complexity.
β’ Leads the statistical programming activities for studies.
β’ Develop SAS programs for the creation of ADaM data sets following CDISC standards.
β’ Develop SAS programs for the creation of Tables, Listings and Figures.
β’ Validation of ADaM data sets, Tables, Listings and Figures.
β’ Create specifications for the structure of ADaM data sets for individual studies and integrated data.
β’ Create documentation for regulatory filings including reviewers guides and data definition documents
β’ Leads the development of standard SAS Macros and participates in the development of standard operating procedures.
β’ Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.
Requirements:
β’ 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.
β’ In-depth understanding of SAS programming concepts and techniques related to drug development.
β’ Fundamental understanding of CDISC Standards.
β’ Fundamental understanding of the drug development process, including experience with regulatory filings.
β’ Ability to communicate clearly both oral and written.
β’ Ability to accurately estimate effort required for study related programming activities.
Additional Information
All your information will be kept confidential according to EEO guidelines.