Statistical Analyst III - Katalyst CRO : Job Details

Statistical Analyst III

Katalyst CRO

Job Location : all cities,IL, USA

Posted on : 2025-07-26T01:21:51Z

Job Description :

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  • Demonstrated practical understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry.
  • Demonstrated satisfactory ability to apply SAS programming knowledge and work independently to solve problems related to non-routine situations.
  • Responsible for the creation and validation of ADaM, TLFs for CSR, ISS, and Client following's SOPs, department, and project standards.
  • Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and resolving Pinnacle 21 checks.
  • Responsible for the creation and accuracy of derivations as defined in the protocol and statistical analysis plan.
  • Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications.
  • Ensure consistency across studies within a project.
  • Responsible for the creation of data definition documents, TOCs, and support submission related activities.
  • Learn and maintain expertise in the use of the utilities and macros developed for the Statistical Programmers.
  • Develop new macros and utilities.
Responsibilities
  • Demonstrated practical understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry.
  • Demonstrated satisfactory ability to apply SAS programming knowledge and work independently to solve problems related to non-routine situations.
  • Responsible for the creation and validation of ADaM, TLFs for CSR, ISS, and Client following's SOPs, department, and project standards.
  • Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and resolving Pinnacle 21 checks.
  • Responsible for the creation and accuracy of derivations as defined in the protocol and statistical analysis plan.
  • Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications.
  • Ensure consistency across studies within a project.
  • Responsible for the creation of data definition documents, TOCs, and support submission related activities.
  • Learn and maintain expertise in the use of the utilities and macros developed for the Statistical Programmers.
  • Develop new macros and utilities.
Requirements:
  • MS in Statistics, Computer Science or a related field with 5 to 7 years of SAS programming experience in Pharmaceutical or related industry. OR
  • BS in Statistics, Computer Science or a related field with 5 to 7 years of SAS programming experience in Pharmaceutical or related industry.
  • Strong experience with clinical trials, including familiarity with expectations of regulatory agencies.
  • Strong working experience/skill in ADaM datasets creation/validation.
  • Strong technical and communication skills, both oral and written.
  • Competent in SAS programming, macro, and utilities development.
  • Good CDSIC knowledge.
  • Provide accurate and timely responses to requests from clients with a sense of urgency.
  • Be compliant with training requirements.
Seniority level
  • Seniority levelMid-Senior level
Employment type
  • Employment typeFull-time
Job function
  • Job functionResearch, Analyst, and Information Technology

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