Description

Key Responsibilities

  • Develop and validate complex analysis datasets (ADaM) and TFLs using SAS.
  • Write and review programming specifications and supporting documentation.
  • Create standard macros and tools to improve efficiency.
  • Serve as a project lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members.
  • Communicate with clients as the key programming contact, including delivering outputs and managing feedback.
  • Conduct SAS code review, track issues, and ensure quality standards are met.
  • Archive all programming deliverables and documentation per SOPs.
  • Mentor team members and support their technical and professional development.
  • Ensure compliance with ICH-GCP, CDISC standards, and company SOPs.

Requirements

  • Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field.
  • 3+ years of SAS programming experience in pharmaceutical or CRO environments.
  • Strong knowledge of clinical trials, statistical methods, and regulatory requirements.
  • Proven experience leading programming projects and mentoring team members.
  • Excellent communication skills and experience working with global teams and clients.
  • Proficient in Microsoft Office and SAS software.