Global Nonclinical Regulatory Strategy & Dossier Author

A global healthcare services provider is seeking a Senior Nonclinical Regulatory Strategist & Submission Author. This role will lead the strategy, planning, and authorship for global regulatory submissions within the pharmaceutical sector. The ideal candidate will possess extensive regulatory experience, project management skills, and a scientific background. Responsibilities include authoring nonclinical sections of submissions, preparing responses to Health Authority queries, and maintaining compliance. Competitive salary range and a wide variety of benefits offered. #J-18808-Ljbffr