Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. * Reviews the study scope of work, budget and protocol content and ensures the clinical (CRAs/Central Monitors) is aware of the contractual obligations and parameters. * Collaborates with other functional such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines. * Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. * Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor
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