• Designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies in the clinical study sites • Acting as the primary contact and clinical trial expert for assigned study site personnel • Performing site assessments and qualification visits to support the site selection decision process • Developing and managing key study site documentation • Participating in and overseeing CRO delivery of site management activities • Validating product performance claims, supplying data for critical regulatory submissions • Executing site management activities for sponsored studies in assigned focus areas across all phases of study • Working in local and global study teams, including virtual teams