Clinical Trial Site Monitoring Oversight Specialist

Job DescriptionPurpose:The purpose of the Lead, Monitoring Oversight role is to be an advocate for monitoring oversight who works with the Clinical Design, Delivery & Analytics (CDDA), the Medicines Quality Organization (MQO) and Investigator Engagement (IE) to ensure that Lilly has appropriate oversight of clinical trial site monitoring activities...

Job Title: Clinical Oversight LeadAbout the RoleThe Clinical Oversight Lead is responsible for ensuring effective clinical trial site monitoring activities. This role works closely with cross-functional teams to ensure Lilly has appropriate oversight of outsourced clinical trial site monitoring.Main Responsibilities:Conduct regular review of Monitoring Visit...

At Lilly we unite caring with discovery to make life better for people around the world We are a global healthcare leader headquartered in Indianapolis Indiana Our employees around the world work to discover and bring life-changing medicines to those who need them improve the understanding and management of disease and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

The role of the Lead Monitoring Oversight is to provide leadership in monitoring oversight activities. This includes working with various teams to ensure that clinical trial site monitoring activities are appropriately overseen.Key ResponsibilitiesConduct Monitoring Visit Report Reviews (MVRRs) and identify any issues or gapsCollate data from multiple...

Job Overview:Centralized Monitoring LeadAs Centralized Monitoring Lead, you will be responsible for providing strategic leadership to a team of professionals in achieving project objectives. Your expertise will ensure the efficient review of site visit reports and consistent quality standards.This role requires a strong understanding of clinical trial...

Job OverviewWe are seeking a skilled and experienced professional to lead our centralized monitoring team. As the Centralized Monitoring Lead, you will be responsible for providing leadership and oversight of clinical deliverables across all trial phases.Key responsibilities include developing and reviewing study management plans, risk assessments, and...

Our company is seeking a skilled professional to take on the role of Site Selection Lead. In this position, you will be responsible for identifying and selecting suitable sites for clinical trials.Key Responsibilities:Develop Initial Site List: Work closely with the Global Feasibility Lead to develop an initial site list for feasibility and site...

Job Overview:The Centralized Monitoring Lead is responsible for overseeing the delivery of project objectives to sponsor satisfaction. The role entails optimizing speed, quality, and cost of delivery in accordance with standard operating procedures, policies, and practices.Key Responsibilities:Oversight of clinical deliverables across all trial phases...