Must have at least 1.5 years of independent monitoring experienceEngage in innovative Immunology and multi Therapeutic Area Clinical TrialsFocus on enhancing quality of life while traveling regionallyExhibit leadership capabilities by contributing to various initiatives and acting as a Subject Matter Expert (SME) in systems and processesMentor and coach junior team membersTake on the role of Lead Study Manager, providing training to other Study Managers on studiesCreate essential site start-up documents including the Site Initiation Visit (SIV) agendaProvide the Study Manager perspective during the review of study documents, such as Monitoring GuidelinesRepresent Lead Trial Managers or Study Managers in various meetings and project teamsAssume responsibilities for reviewing reports (SQV, SMV, SCV) for sites managed by other Study Managers within the same trialAssist in the development of country budgets and contract negotiations in collaboration with Clinical Contract Specialists (CCS)Support and assist in conducting the Activation Site Visit (ASV)Metrics and KPIs will be managed according to the Quality Oversight Plan (QOP) document.At ICON, we prioritize inclusion and belonging as core components of our culture and values. We are committed to providing an inclusive and accessible environment for all candidates. ICON is dedicated to ensuring a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.