Clinical Study Lead

As a Clinical Study Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be responsible for vendor oversight for adherence to budget, timelines and organizational objectives of individual protocols/programs. Develops strong vendor and site relationships and ensures continuity of relationships through all phases of the trial. Coordinates & manages various tasks in collaboration with other sponsor roles to achieve site readiness. You will perform timely review of monitoring reports from CRO and associated deliverables demonstrating sponsor oversight, and perform periodic reviews of the CRO eTMF/TMF to ensure adherence with standards and compliance with the relevant regulations and guidelines. You will support financial management of the study which includes review and approval of site and vendor invoices and risk Management initiatives. You will also Maintain clinical trial registry entry/updates, as required and provide mentorship/guidance to junior team members or cross-functional colleagues on study processes/study requirements.