Clinical Research Coordinator

Coordinate and manage clinical trial activities in compliance with study protocols, Good Clinical Practice (GCP), and FDA/ICH regulations. (Multiple positions available.) Coordinate and manage clinical trial activities in compliance with study protocols, Good Clinical Practice (GCP), and FDA/ICH regulations, while adhering to all regulatory and ethical requirements. Recruit, screen, and enroll study participants; obtain informed consent; and verify subject eligibility in accordance with study protocols and institutional guidelines. Collect, document, and maintain accurate clinical research data in Case Report Forms (CRFs) and electronic data capture systems; monitor data quality and ensure timely reporting of adverse events, protocol deviations, and compliance issues. Assist in preparing study documentation, reports, and submissions for Institutional Review Boards (IRBs), sponsors, and regulatory authorities as required. Collaborate with investigators, sponsors, and clinical staff to support study progress, site monitoring, and audits. Coordinate and conduct study-related training for clinical and administrative staff, ensuring consistent protocol adherence, proper documentation practices, and smooth execution of trial activities. Requirements Bachelor's degree in Biotechnology, Neuroscience, Life Sciences, or a related field, or a foreign equivalent. Note #J-18808-Ljbffr TechMetro