Lead Statistical Programming for NDA Submissions

A biopharmaceutical company in South San Francisco is looking for an experienced Senior Manager in Statistical Programming to lead statistical program development for clinical studies. The ideal candidate will have expert-level SAS programming skills, experience with CDISC standards, and a strong background in drug development. This role focuses on ensuring quality deliverables while adhering to regulatory requirements, contributing to important drug development efforts. Candidates should have a minimum of 8 years in the field and effective communication skills. #J-18808-Ljbffr