Description

Key Responsibilities

  • Act as lead programmer for large, global, or high-complexity clinical projects.
  • Provide expert-level programming guidance to internal teams and clients.
  • Drive process optimization and programming standardization across the department.
  • Solve critical technical issues, and develop standard macros and tools to enhance team efficiency.
  • Deliver advanced technical training to team members.
  • Mentor and support junior programmers and mid-level staff.
  • Take a hands-on leadership role in project execution and communication with clients.

  • Requirements

    • Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field.
    • 8+ years of SAS programming experience in clinical trials within pharma or CRO settings.
    • Proven experience leading large and complex projects in a programming function.
    • Strong leadership, strategic thinking, and team management skills.
    • Expert in SAS programming with solid statistical knowledge of clinical trials.
    • Effective verbal and written English communication skills.
    • Proficient in statistical tools.