IQVIA - Overland Park, KS
posted 3 months ago
As a Clinical Research Associate (CRA) at IQVIA, you will have the opportunity to develop your career in a dynamic and supportive environment. This role is designed to be a stepping-stone into various career paths, including operations management, dedicated customer solutions, and project management. At IQVIA, we believe in removing career ceilings, allowing you to explore and progress in your career without limitations. You will receive dedicated mentoring and structured quarterly reviews to assess your performance, with opportunities for promotions and bonus awards. Our innovative approach includes access to cutting-edge in-house technology, enabling you to work on global projects while maintaining a regional or home state travel remit, eliminating the need for extensive national travel in certain countries. Your responsibilities will include performing site selection, initiation, monitoring, and close-out visits, as well as maintaining appropriate documentation throughout the clinical trial process. You will support the development of subject recruitment plans and establish regular lines of communication with assigned sites, administering protocol and related study training. Evaluating the quality and integrity of site practices will be crucial, and you will be responsible for escalating quality issues as necessary. Additionally, you will manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and resolving data queries. This role requires strong collaboration and communication skills, as you will interact with a variety of colleagues and customers. A solid understanding of applicable clinical research regulatory requirements is also essential.