CRC-Avacare

Conduct clinical research site activities in accordance with regulations, SOPs, and protocols, including assisting with feasibility surveys, site initiation, and subject screening and enrollment. Manage trial medications, study materials, and laboratory samples while coordinating follow-up steps and data entry into case report forms. Participate in investigator meetings, monitoring visits, and audits, then archive study documents and submit them to ethics committees. Execute site closure procedures involving visit completion, material recovery, and final data archiving. Create daily work reports and complete assigned tasks. Requires a bachelor's degree in clinical medicine, pharmacology, nursing, or related fields; clinical research experience preferred. IQVIA accelerates the development of innovative medical treatments to improve patient outcomes and population health worldwide.