as an Associate Director, US Advertising & Promotion Regulatory Review out of our Lexington, MA or Exton, PA office... with the planning and prioritization of proposed promotional and disease state materials. Collaborate with Regulatory Affairs...
as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will serve as an internal expert on FDA regulations, guidance..., you will report to the Director, Ad/Promo Regulatory Review. You will be based in either our Lexington, MA or Exton, PA home office...
) to receive an alert: × Select how often (in days) to receive an alert: Senior International Medical Director Facility... Director serves as a subject matter expert for our products and related data within a therapeutic area. The Senior...
to make a difference? The Position The Senior International Medical Director serves as a subject matter expert... for our products and related data within a therapeutic area. The Senior International Medical Director is a team player, detail...
Reports to: Senior Medical Director, GNAT Early Clinical Development. Work with the Early Development Medical and Science... Group, whose functions include Drug Safety, Regulatory Affairs, Clinical Operations, Medical Writing, Biostatistics, Data...
experts, and Principal Investigators. Relationships Reports to: Senior Medical Director, GNAT Early Clinical Development... functions in the Novo Nordisk US Clinical Development Group, whose functions include Drug Safety, Regulatory Affairs, Clinical...
clinical development and regulatory requirements of a clinical program. Relationships The Senior Medical Writer reports... to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal...
of a clinical program. Relationships The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical.... Are you ready to make a difference? The Position The Senior Medical Writer works closely with cross-functional project teams...