Global Nonclinical Regulatory Strategy & Dossier Author

A healthcare solutions company in South Dakota is seeking a Senior Nonclinical Regulatory Strategist to lead strategy and authorship for global regulatory submissions. The ideal candidate will have over 7 years of regulatory experience, strong project management skills, and a scientific background. Responsibilities include authoring nonclinical sections of registration dossiers and preparing responses to health authority queries. This full-time position offers competitive compensation and benefits, including medical coverage and flexible spending accounts. #J-18808-Ljbffr