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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.