Job Description

Key Deliverables:

  • Develop and validate SAS programs for clinical reports and regulatory submissions
  • Create SDTM and ADaM datasets per CDISC standards
  • Generate statistical TLFs for internal/external reporting
  • Maintain and troubleshoot clinical reporting systems

Role Responsibilities:

  • Collaborate with biostatisticians and data managers to gather requirements
  • Perform clinical data analysis and ensure data quality
  • Adhere to FDA and industry-compliant documentation practices
  • Respond to ad hoc data and reporting requests swiftly


Skills Required
Sas, ADAM, clinical data analysis , Sas Macros

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