As a Clinical Study Support Specialist, you will organize and deliver 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. The role involves collating data for assessments such as feasibility and site selection, contributing to the review of study documents and manuals, and tracking site activation and enrollment.
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Provides overall support to study sites and clinical project teams engaged in clinical research studies, adhering to applicable protocols, SOPs, and regulatory requirements. Acts as point of contact for study sites and expected to work independently in providing support to CRA and sites. Can have increased focus on training and development of junior staff members and can act as Lead In-house CRA.