Clinical Research Coordinator
CurrentResearch Office & Department of General Medicine (Infectious Disease)➢ Directly involved in studies recruitment, biological sample collection, subjects’ follow-up, data entry, maintenance of study site files, CIRB submissions and other study-related as required➢ Ensure full quality, accuracy and completeness of data collection➢ Monitor subject’s compliance to their treatment and follow-up➢ Managing feasibility studies➢ Monitoring adverse events and safety reporting➢ Assist in budget preparation, facilitate clinical trial agreements & study-related expenses➢ Collaborating between key stakeholders of research studies including PIs, other site members from other institutions and industry partners➢ Collaborating with clinical research teams to ensure data is accurately and consistently collected ➢ Developing and implementing data management plans, including data cleaning, validation, and verification procedures.➢ Ensuring data is in compliance with regulatory requirements and industry standards➢ Preparing and submitting regulatory reports and study documents to regulatory agencies.