Research Assistant

Research Assistant provides administrative and clinical support at the study site to ensure study activities are performed in accordance with the protocol and regulatory requirements. Responsibilities include prioritizing tasks in a fast-paced environment, identifying and reporting protocol deviations and adverse events (AEs), ensuring compliance with GCP and FDA regulations, assisting with subject retention, inventory management, meticulous documentation, laboratory duties (proper labeling, handling, storage, and shipment of specimens), and maintaining patient rapport and data collection for clinical drug trials. The role requires ability to follow detailed instructions, handle confidential information, and adapt to evolving study requirements; occasional weekend or overtime hours may be required; reports to the Site Manager/Team Lead; non-exempt classification.