Global Nonclinical Regulatory Strategy & Dossier Author

A global healthcare services company based in Indianapolis is seeking a Senior Nonclinical Regulatory Strategist & Submission Author. This role focuses on leading the strategy, planning, and authorship of nonclinical components for regulatory submissions. The ideal candidate will have at least 7 years of nonclinical regulatory experience and a strong understanding of pharmaceutical sciences and drug development processes. The salary range is competitive, and benefits include medical coverage, paid time off, and a 401k plan. #J-18808-Ljbffr