Statistical Programmer Job at Katalyst CRO, Chicago, IL

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  • Katalyst CRO
  • Chicago, IL

Job Description

Overview

Join to apply for the Statistical Programmer role at Katalyst CRO .

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 SDTM, ADaM and TLFs for CSR, ISS, and Client following SOPs, department, and project standards.
  • Ensure internal consistency of output and assess consistency with other activities for the project (e.g., ISS, Client), as applicable.
  • Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and resolving Pinnacle21 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.
  • Provide accurate and timely responses to requests from clients with a sense of urgency.
  • Be compliant with training requirements.
Requirements
  • MS in Statistics, Computer Science, or a related field with 3+ years of SAS programming experience in Pharmaceutical or related industry OR BS in a related field with 5+ years of SAS programming experience in Pharmaceutical or related industry.
  • E-sub experiences (CDISC dataset, creating define file, etc.).
  • Strong experience with clinical trials, including familiarity with expectations of regulatory agencies, especially FDA and EMEA.
  • Strong working experience/skill in SDTM and ADaM datasets creation/validation.
  • Strong technical and communication skills, both oral and written.
  • Competent in SAS programming, macro, and utilities development.
Seniority level
  • Mid-Senior level
Employment type
  • Contract
Job function
  • Information Technology
Industries
  • Pharmaceutical Manufacturing

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Job Tags

Contract work, Work experience placement,

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