A dynamic leader with 20+ years experience in Pharmaceutical Research, including 16 years in Project Management and Clinical Operations. A strategic thinker with strong industry perspective in an expansive range of therapy areas across the full drug development lifecycle.
Have successfully directed a variety of complex global programs ranging from CMC drug development/manufacture to Phase I and bioequivalence studies, Phase II proof of concept studies, Phase III clinical trials and Phase IV/peri-approval, observational, health economic studies. Serving as the primary liason between global operational stakeholders, very proficient in leading cross-functional teams in the planning, executing, and monitoring of drug development research projects against scope, budget, timeline, resource, and quality metrics. Work effectively across multiple divisions to direct the delivery of projects/programs. Provide direct supervision, support, and training to full clinical operations and data technology staff. Responsible for developing and maintaining effective stakeholder relationships.
Very experienced in commercial/business aspects of research operations. (business & proposals development). Collaborating with senior executives and as liaison with business development, responsible for operational strategy, budgets, and acquisition of new business.