Clinical SAS Programmer

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profile Job Location:

Detroit, MI - USA

profile Monthly Salary: Not Disclosed
Posted on: 29-08-2025
Vacancies: 1 Vacancy

Job Summary

Responsibilities:
  • Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
  • Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets.
  • Creates and validates tables figures and listings (TFLs) in a timely and high-quality fashion consistently meeting objectives of the study and regulatory requirements.
  • Provides input in the design and development of case report forms and clinical databases.
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets ADaM datasets and TFLs.
  • Programs for quality checks for clinical study raw data and report the findings to Data Management.
  • Provides input in the design and development of case report forms and clinical study databases.
  • Reviews or author aCRF SDTM and ADaM datasets specifications for datasets programming.
Requirements:
  • MS in Statistics Computer Science or a related field with at least 3 years or BS in Statistics Computer Science or a related field with at least 5 years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • Ability to work on a multidisciplinary team that may include Biostatistics Medical Directors Data Management Medical Writing Pharmacovigilance Clinical Operations Medical Affairs etc.
  • Ability to prioritize and multi-task effectively.
  • Demonstrated positive attitude and the ability to work well with others.
Responsibilities: Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets. Creates and validates tables figures and listings (TFLs) in a timely...
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Key Skills

  • Databases
  • SQL
  • FDA Regulations
  • R
  • Relational Databases
  • Data Management
  • Data Structures
  • Clinical Trials
  • Statistical Software
  • CDISC Standards
  • SAS
  • Oracle