Clinical Research Coordinators Salary in Atlantic City, NJ

Common tasks

• Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
• Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
• Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
• Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• Inform patients or caregivers about study aspects and outcomes to be expected.
• Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
• Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
• Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
• Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
• Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.