Found Description
About ICONWe are a global clinical research organization dedicated to advancing patients' lives.Role SummaryLead clinical trial start‐up activities by understanding client objectives and assisting in developing plans for country and site distribution.ResponsibilitiesOversees day to day delivery of all aspects of site activation in the projects assigned.Ensures that each project has a site activation plan and that the study is being conducted in accordance with that plan, meeting sponsor timelines and expectations, and complying with ICON/client KPIs, SOPs, reporting norms and regulatory requirements.Leads sponsor initiatives such as kick‐off meetings, bid defenses, project update and status calls, and other communications.Utilizes project management skills to optimize performance and collaboration to ensure successful study outcomes.QualificationsBachelor's Degree preferably in life sciences.Minimum 2+ years of experience in a clinical research environment, focusing on start‐up acti...