Description
The role supports clinical development projects by coordinating project start-up activities, creating global programs, tracking spreadsheets, and producing and quality-checking SAS-derived datasets, tables, figures, and data listings. It also maintains regulatory and CDISC knowledge, provides training and mentorship, supports submission documentation, and ensures compliance with SOPs, ICH-GCP, and applicable regulations. The position requires SAS proficiency, analytical and communication skills, attention to detail, and the ability to work in a global, quality-focused environment.
