*Roles and Responsibilities Provides regulatory expertise and support for pre-clinical and clinical areas for investigational products for the treatment and diagnosis of tuberculosis. Manages the development of global regulatory strategy and ensures the quality and timely production of dossiers for global submission. Oversees the writing, production and ensures the quality of key clinical and regulatory documents for TB products. Partners with local regulatory staff in OPDC, OPC-J, OFRI, and ot
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