Clinical Trials Research Coordinator

Clinical Coordinator, Clinical Program Coordinator, Clinical Program Manager, Clinical Research Administrator, Clinical Research Coordinator, Clinical Research Manager, Clinical Research Nurse Coordinator, Clinical Trial Coordinator, Clinical Trial Manager, Research Coordinator

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.

• 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 the 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.

• Active Listening — Giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times.
• Reading Comprehension — Understanding written sentences and paragraphs in work-related documents.
• Writing — Communicating effectively in writing as appropriate for the needs of the audience.
• Coordination — Adjusting actions in relation to others' actions.
• Speaking — Talking to others to convey information effectively.