Clinical Research Associate I

Working remotely, the full-time Clinical Research Associate I will monitor clinical investigative sites to ensure adherence to protocols, conduct site visits for Phase 1-4 studies, and manage investigator payments while ensuring compliance with regulations and quality standards. Key responsibilities: Monitor activities at clinical sites to ensure successful execution of study protocols and compliance with regulations Conduct site qualification, initiation, monitoring, and closeout visits in accordance with Good Clinical Practices and AbbVie SOPs Train site personnel on protocols and regulatory requirements while managing investigator agreements and payments Required qualifications: Appropriate tertiary qualification in a health-related field (e.g., Medical, Scientific, Nursing) preferred, with a Clinical Trials Master's Degree Minimum of 1 year of clinically-related experience, including 6 months in independent clinical research monitoring or as a Study Coordinator In-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines, and applicable regulations Strong planning and organizational skills to manage competing projects and deadlines effectively Ability to communicate clearly and address clinical site issues with appropriate guidance