Statistical Programming Associate Director

Role: Associate Director of Statistical Programming overseeing quality and timely delivery of programming for clinical development. Responsibilities: lead full project scope, ensure high-quality deliverables, manage external partners (e.g., CROs), drive process improvements, develop best practices, and provide technical mentorship within the programming discipline. Qualifications: degree in Mathematics, Statistics, Computer Science, or Life Sciences; proven programming expertise; strong industry knowledge of clinical development processes, standards, and regulatory requirements; ability to influence stakeholders and manage risks. Preferred skills include planning and organizational abilities. High-Value: role supports early-stage to late-stage clinical trials, emphasizing automation, standards development, and cross-functional collaboration in a regulated biopharma environment. Location: Durham, NC, with in-office expectations at least three days/week; flexible work arrangements. Salary range: $137,135-$205,703, with incentives and comprehensive benefits.