Global Nonclinical Regulatory Strategy & Dossier Author

A global healthcare services company is seeking a Senior Nonclinical Regulatory Strategist & Submission Author to lead nonclinical strategy for regulatory submissions. This role requires extensive experience in nonclinical regulatory processes and strong project management skills. Responsibilities include authoring registration dossiers and preparing responses for Health Authority inquiries. Candidates should possess a scientific degree and have a thorough understanding of global nonclinical regulations. Bonuses and comprehensive benefits package are included. #J-18808-Ljbffr