Manager - Statistical Programming
Core
Design, develop, and implement technical solutions for integrating, analyzing, and reporting clinical data to support product development and regulatory approval.
Role type
Senior IC statistical programmer (clinical data)
Builds
Clinical trial data analysis and reporting deliverables
Domain
Pharmaceutical clinical development / Biostatistics
Deliverable
production ML models | dashboards & analysis
Required skills
SAS programming (Base, Stat, Graph), clinical trial methodology, regulatory requirements knowledge, cross-functional collaboration, project prioritization
Preferred skills
Oncology experience, globalization of processes
Technologies
SAS
Responsibilities
Develop programming strategies and specifications; review planning documents for alignment; communicate with project leadership and vendors; ensure quality of deliverables per regulatory standards; identify efficiency opportunities; support candidate technical evaluation
Seniority
Senior, hands-on IC
