Global Nonclinical Regulatory Strategy & Dossier Author

A health services company in Nashville, TN, is seeking a Senior Nonclinical Regulatory Strategist to lead the strategy and authorship of nonclinical components for global submissions. This role involves working with cross-functional teams to ensure compliance with global regulations, author various modules for drug applications, and manage interactions with Health Authorities. Candidates should have over 7 years of regulatory experience and a relevant scientific degree. Competitive salary and benefits package offered. #J-18808-Ljbffr