Principal Consultant
Ken McFarlane is a Principal Consultant at Medidata and has 20 years of experience in clinical research, primarily in the areas of clinical trial management, monitoring, site activation, and site contracting, with direct experience as a Sponsor and working with Sponsors through CROs.
Prior to joining Medidata, Ken spent the majority of his career at a global CRO where he led global project management and site monitoring teams, and oversaw global study start-up and trial master file groups. In addition to direct project management and monitoring experience in Phases I-IV studies, he has also led a variety of cross-functional organizational initiatives aimed at advancing process optimization, driving innovation, technical mentoring, and fostering change management.