Description
AstraZeneca is hiring a Nonclinical Document Specialist to support the Nonclinical Submission group by preparing, editing, and maintaining regulatory submissions for clinical trial and marketing applications. The role covers nonclinical dossier structures, regulatory-authority requirements, electronic document management, archival data, CTD and GXP standards, and submission-ready documentation. Candidates need experience with pharmaceutical document systems such as Veeva Vault, regulatory submission tools, Microsoft Office, SharePoint, and process automation, along with a bachelor’s degree or equivalent industry-relevant experience. The posting states that employees work at least three days per week from the office and provides a closing date of 13-out.-2026.
