Tasks of a Clinical Research Coordinator: - Study Planning: Collaborating with the research team to develop study protocols, including participant recruitment strategies, data collection methods, and study timelines. - Participant Recruitment: Identifying and screening potential participants, obtaining informed consent, and enrolling eligible individuals into the study. - Data Collection: Collecting and recording data from study participants through interviews, medical examinations, and laboratory tests, ensuring accuracy and adherence to protocols. - Data Management: Organizing and maintaining study data, ensuring confidentiality and compliance with regulatory requirements. - Study Monitoring: Monitoring study progress, identifying and addressing any issues or deviations from protocols, and reporting to the principal investigator. - Adverse Event Reporting: Promptly reporting any adverse events or serious adverse events to the appropriate authorities and ensuring participant safety. - Quality Control: Conducting regular quality control checks to ensure data integrity and adherence to good clinical practices. - Documentation: Preparing and maintaining study documentation, including case report forms, study logs, and regulatory submissions. - Collaboration: Liaising with study sponsors, regulatory agencies, ethics committees, and other stakeholders to ensure compliance with regulations and study requirements. - Training: Providing training and guidance to study staff, ensuring their understanding of study protocols and procedures. - Study Closure: Assisting with study closure activities, including data analysis, final reporting, and archiving study documents. Please note that the specific tasks may vary depending on the nature of the clinical research and the organization's requirements.