Steve Sibley
Pharma
Certara
Japan
Biography
With a career spanning more than 25 years in the pharmaceutical industry, Mr. Sibley has extensive experience across regulatory writing, consulting, and clinical project leadership roles. He has successfully supported projects from discovery through approval and life cycle management. These include significant roles in more than 50 submissions and, in several cases, leading the entire submission team overseeing all documentation from Modules 1 through 5. Mr. Sibley drives the expansion of the company’s submission leadership and consulting capabilities in guiding clients to successful clearance of regulatory milestones.
Research Interest
Healthcare
