Director 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.

Coordinates the preparation and life-cycle management of nonclinical regulatory documents from early development through post-marketing. Highly collaborative role involving coordination of document logistics and deliverables across multi-functional groups. In addition, provides input and guidance towards strategic execution of global Health Authority guidelines as they pertain to nonclinical submissions.