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Job Description
Structured overview of role & requirementsAbout This Role
Lead and manage statistical programming for one or multiple clinical studies as Study Lead Programmer, overseeing end-to-end delivery and compliance.
Develop programming strategies and specifications (e.g., SDTM, ADaM) and coordinate cross-functional activities including data quality and regulatory submission support.
Provide technical leadership, manage programmer assignments, and ensure consistent and timely high-quality deliverables across projects.
Minimum Requirements
Bachelor's degree or higher in biostatistics, statistics, mathematics, computer science, or related quantitative/scientific field.
At least 6 years of statistical programming experience in a clinical development environment.
Strong knowledge of clinical trial processes and CDISC standards (SDTM, ADaM, Define).
Advanced SAS programming skills including SAS/STAT; excellent project management and communication skills.
Ideal Candidate Profile
Experienced in leading and managing statistical programming teams through the full study lifecycle in a global clinical development setting.
Technical expertise in clinical data standards and programming best practices to drive compliance and quality.
A hands-on programming leader who balances team management with direct contribution to complex programming deliverables.