CPM is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies in compliance with Novartis processes and regulatory requirements. Minimum 5 years’ experience in clinical research in a role that oversees (project management) and/or with monitoring clinical trials. Strong project management capabilities with demonstrated ability to problem solve and mediate complex issues.