Clinical Research Coordinator

Company Description DaVinci Research is dedicated to clinical research trials, working in collaboration with leading pharmaceutical and medical device companies worldwide. As a Site Management Organization, we bridge the gap between Investigators and study sponsors to ensure the successful completion of clinical trials. Our commitment lies in advancing medical research and fostering innovation in the healthcare industry. Role Description This is a full-time on-site role for a Clinical Research Coordinator located in Roseville, CA. The Clinical Research Coordinator will manage the day-to-day activities of clinical trials, including obtaining informed consent, following study protocols, and coordinating with research teams. Responsibilities include ensuring adherence to regulatory requirements, maintaining accurate records, and facilitating communication between investigators and study sponsors. Qualifications Experience with Informed Consent and Protocol adherenceBackground in Research and Clinical TrialsClinical Research ExperienceExcellent organizational and multitasking skillsStrong communication and interpersonal abilitiesAbility to work on-site in Roseville, CABachelor’s degree in a related field or equivalent experience