Clinical Study Specialist

As a Clinical Study Support Specialist, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This role involves organizing and delivering analyzable reports and metrics to the clinical study lead. You will schedule and coordinate meetings, prepare agendas, presentation materials and minutes for clinical study team meetings and other study related meetings. You will also collate data for assessments such as feasibility and site selection, and contribute to the review of study documents such as informed consent forms and case report forms. The role also includes tracking site activation, enrolment, and monitoring visits to projected plans, escalating any issues or delays. Scheduled reconciliations of the study Trial Master File (TMF) and maintaining team SharePoint sites are also part of the responsibilities. The specialist may manage or contribute to oversight of Third Party Vendors (TPV) and participate in Standard Operating Procedures (SOPs) revisions or departmental initiatives.