3+ years of specific project management experience in one or more of the following: drug development and commercialization, CMC, regulatory submission and/or regulatory compliance and quality assurance and medical device product development.
5+ years of experience in the medical device or pharmaceutical industries.
Knowledge and application of disciplined project management processes and tools – Project Management Professional (PMP) certification is a plus
Exceptional interpersonal and leadership skills
Strong communication skills
Strong computer skills in MS Project, PowerPoint, Excel and Visio
Ability to produce and present clear, concise, and professionally written communications
Capable of working independently
Bachelor’s degree in a science, engineering or business discipline. Advanced degrees are a plus.