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.
• 5+ years of SAS programming experience in pharmaceutical or CRO environments.
• Solid 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 SAS software.