Clinical Research Coordinator - 253921

Key ResponsibilitiesAssist with research department operations including SOP development, department start-up activities, equipment ordering, invoicing, expense tracking, and study feasibility assessmentsResearch new study and business opportunities through government and industry resources such as ClinicalTrials.govCoordinate assigned clinical trials, including managing timelines, budgets, study documentation, and regulatory requirementsSupport patient recruitment, screening, informed consent, and retention effortsConduct protocol reviews and communicate study requirements, inclusion/exclusion criteria, and protocol updates to research staff and applicable departmentsCollect, organize, and maintain accurate clinical research data; perform data entry, query resolution, and quality checksEnsure study staff are trained on protocols, electronic systems, and study proceduresAttend sponsor meetings and study trainings and communicate study expectations to internal teamsAssist in mentoring and supporting research staff while promoting a collaborative team environmentCoordinate with internal departments, sponsors, and IRBs to ensure smooth study execution and compliance with GCP and institutional guidelinesQualificationsBachelor's degree in a scientific, healthcare, or research-related field preferredPrior clinical research experience as a Clinical Research Coordinator, Research Assistant, or similar role requiredGCP, ACRP, and/or IATA certification preferred or willingness to obtain certificationStrong understanding of clinical research processes, SOPs, and regulatory requirementsExperience with EMR systems, electronic data capture platforms, and clinical documentationExcellent organizational, communication, and project management skills with the ability to manage multiple studies simultaneously