Clinical Research Coordinator

This is a full-time Clinical Research Coordinator. The Clinical Research Coordinator will be responsible for overseeing and managing clinical research studies, coordinating recruitment and enrollment of study participants, executing informed consent processes, and managing study protocols. Additional tasks include ensuring compliance with applicable regulations, facilitating communication between study teams, maintaining research documentation, and providing support in the execution of high-quality clinical trials. Qualifications Comprehensive knowledge and experience with Informed Consent processes and Protocol adherence Strong background in Research and Clinical Research Experience Proficiency with Clinical Trials processes and conducting them in compliance with guidelines Strong organizational, communication, and attention-to-detail skills Ability to work independently in a remote setting and manage multiple priorities Knowledge of Good Clinical Practice (GCP) guidelines and applicable regulatory requirements Experience with electronic data capture (EDC) systems is a plus Bachelor's degree in life sciences, healthcare, or a related field preferred #J-18808-Ljbffr