Global Nonclinical Regulatory Strategy & Dossier Author

A healthcare services company in Topeka, Kansas is seeking a Senior Nonclinical Regulatory Strategist & Submission Author to lead the strategy, planning, and authorship of nonclinical components for global regulatory submissions. The ideal candidate should possess at least 7 years of nonclinical regulatory experience, a Bachelor's degree in a scientific discipline, and exhibit strong project management and leadership skills. Join us to ensure compliance and high-quality submissions within a dynamic team environment. #J-18808-Ljbffr