Global Nonclinical Regulatory Strategy & Dossier Author

A leading healthcare company is seeking a Senior Nonclinical Regulatory Strategist & Submission Author to lead strategy and authorship for global regulatory submissions. The ideal candidate will have at least 7 years of regulatory experience, strong project management skills, and expertise in preparing nonclinical sections of registration dossiers. Responsibilities include authoring CTD modules, developing nonclinical strategies, and ensuring compliance with global regulations.

A competitive salary range of $123,400 - $176,300 is offered, alongside an attractive benefits package.
#J-18808-Ljbffr