{"c":"11-9121.01","n":"Clinical Research Coordinators","d":"Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.","g":"11","tasks":[{"t":"Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.","core":true,"id":15612,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.","core":true,"id":15587,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.","core":true,"id":15610,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.","core":true,"id":15595,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Inform patients or caregivers about study aspects and outcomes to be expected.","core":true,"id":15602,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.","core":true,"id":15594,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.","core":true,"id":15613,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Oversee subject enrollment to ensure that informed consent is properly obtained and documented.","core":true,"id":15597,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.","core":true,"id":15614,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.","core":true,"id":15603,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.","core":true,"id":15593,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.","core":true,"id":15608,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.","core":true,"id":15592,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Code, evaluate, or interpret collected study data.","core":true,"id":15609,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Direct the requisition, collection, labeling, storage, or shipment of specimens.","core":true,"id":15605,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.","core":true,"id":15601,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.","core":true,"id":15600,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.","core":true,"id":15585,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Order drugs or devices necessary for study completion.","core":true,"id":15598,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Contact outside health care providers and communicate with subjects to obtain follow-up information.","core":true,"id":15606,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Participate in the development of study protocols including guidelines for administration or data collection procedures.","core":true,"id":15596,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Confer with health care professionals to determine the best recruitment practices for studies.","core":true,"id":15591,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Communicate with laboratories or investigators regarding laboratory findings.","core":true,"id":15607,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.","core":true,"id":15583,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Organize space for study equipment and supplies.","core":true,"id":15599,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Develop advertising and other informational materials to be used in subject recruitment.","core":true,"id":15589,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.","core":false,"id":15604,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Arrange for research study sites and determine staff or equipment availability.","core":false,"id":15611,"r":52,"dt":"08/2021","src":"Incumbent"},{"t":"Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.","core":false,"id":15588,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.","core":false,"id":15590,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Register protocol patients with appropriate statistical centers as required.","core":false,"id":15584,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Solicit industry-sponsored trials through contacts and professional organizations.","core":false,"id":15582,"r":53,"dt":"08/2021","src":"Incumbent"},{"t":"Participate in preparation and management of research budgets and monetary disbursements.","core":false,"id":15586,"r":53,"dt":"08/2021","src":"Incumbent"}]}