Clinical Research Coordinator

Clinical Research Coordinator IIThe Clinical Research Coordinator is responsible for supporting the management and oversight of clinical trials. This role involves working closely with a team to ensure the smooth execution of research studies under the guidance of the Site Operations Manager.About the RoleEssential Functions:Overseeing Clinical Trials Ensure trouble-free running of clinical trials.Monitor study participants’ health throughout the trial.Compile reports summarizing the success or failure of drugs, technologies, or medical procedures.Oversee 3-4 trials.Data Collection and Analysis Collect data obtained from research.Analyze research data.Participant Interaction Communicate with study participants regarding study objectives.Administer questionnaires.Monitor participant adherence to study rules.Collaboration and Compliance Liaise with laboratories.Monitor study compliance with protocols and ethical standards.Ensure adherence to regulatory requirements.Record Keeping Maintain research records, including case report forms and drug dispensation records.Direct specimen collection, labeling, storage, and transport.Logistics and Supplies Ensure all necessary equipment and supplies are in stock and functional.QualificationsEducation: Bachelor's degree preferred in health-related fieldExperience: 2-year experience in Clinical Research: Must have at least 2 years of experience working on-site directly with patients!Must have study start up, enrollment, and closeout experience. Equal Opportunity StatementWe are committed to diversity and inclusivity.