• Clinical Trial Project Manager and Clinical System End User Support Manager for large global and local phase I - IV trials. Strong ability with clinical systems and metrics.• Accountable for leadership and support of global cross-functional matrix teams, central and local IRB, investigator sites, vendors, budget, clinical data, clinical quality assurance, timelines and deliverables from feasibility to study close out. • Author protocol, amendments and site memos. Review clinical study reports and visit reports. Develop and deliver study and system training to cross-functional teams. Lead communication initiatives with vendors, sites, monitors and stakeholders. Plan and execute global investigator meetings.• Multiple therapy areas including oncology, gastrointestinal, cardiovascular, bone. Large bandwidth of experience across many functional areas.• Knowledge of FDA, ICH-GCP and drug development processes. Strong communicator. Project Management.• CRO, contract, and permanent experience in mid to large pharmaceutical environments. • Travel and relocation will be considered