The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. * Performs qualification, initiation, interim, and close-out visits both remotely and onsite, ensuring proper documentation of monitoring visits. * Works closely with in-house CRAs/CTC and data management to resolve queries on discrepant data. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS). * US: 3 years of experience in the pharmaceutical / biotechnology / CRO industry, 2 year of clinical monitoring experience with 1 year of management experience * Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills
mehr