Xeris Pharmaceuticals Inc. is seeking a Manager, Regulatory Affairs to lead regulatory activities supporting global clinical trials across all phases.
You will prepare and review submissions (INDs/CTAs), help shape regulatory strategy, and interact with internal and external stakeholders to ensure compliance with global health authority requirements. The role requires 5+ years in pharma/biotech with IND/CTA experience, a strong grasp of FDA/EMA/ICH/GCP, and excellent communication.
#J-18808-LjbffrGlobal Regulatory Affairs Lead — Submissions & Strategy in ga at Unknown Company
This position is listed as full time and onsite.