Director, Regulatory Submission And Document Management - Preclinical Development At Merck
CurrentDirector of activities for regulatory submissions and document management within preclinical development at Merck. Oversees the coordination, preparation and life-cycle management of regulatory documents from early development through post-marketing involving coordination of document logistics and deliverables across multi-functional groups. Regulatory resource for navigating and operationalizing global health authority guidelines and requirements across the Merck network.
May 2021 - Present
