Seeking experience in Medical Affairs leadership with background in immunotherapy and vaccine development to support new product launch activities for novel vaccines for infectious diseases.
Must be able to:
*** Review and approve documents and marketing materials including patient information booklets, pharmacology and toxicology sections of regulatory documents, white papers, brochures, ...
Responsible for the development of regulatory business, in accordance with Global RegulatoryAffairs business plans....
Jul 22 - United States
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