• Represents and leads the study team to design, develop and deliver the clinical study to agree upon timelines • Leads planning and communication with cross-functional teams to ensure proper execution and conduct of the clinical trial • Serves as primary contact and resource for CRO and vendor personnel in overarching functions • Provides oversight and management of CROs, consultants and vendors • Monitors progress of clinical activity and reports on the progress of assigned clinical trials including budget and timelines • Prepares potential investigator site lists and assists with their evaluation for inclusion in the study • Participates in meetings – i.e. Study Team Meetings, Investigator Meetings, Monitors’ workshops and CRO Training