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How do they match:
Clinical Research Coordinators
4
Alternate Occupation Titles
Clinical Operations
Specialist
Clinical Research
Specialist
Clinical Support
Specialist
Clinical Trials
Specialist
8
Tasks
Collaborate with investigators to prepare presentations or reports of clinical study
procedures
, results, and conclusions.
Contact industry representatives to ensure equipment and software
specifications
necessary for successful study completion.
Instruct research staff in scientific and
procedural
aspects of studies including standards of care, informed consent
procedures
, or documentation
procedures.
Participate in the development of study protocols including guidelines for administration or data collection
procedures.
Perform
specific
protocol
procedures
such as interviewing subjects, taking vital signs, and performing electrocardiograms.
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or
specially
designated review groups.
Prepare study-related documentation, such as protocol worksheets,
procedural
manuals, adverse event reports, institutional review board documents, or progress reports.
Schedule subjects for appointments,
procedures
, or inpatient stays as required by study protocols.
2
Detailed Work Activities
Advise customers on technical or
procedural
issues.
Develop organizational methods or
procedures.
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How do they match: 11-9121.01 - Clinical Research Coordinators
by
U.S. Department of Labor, Employment and Training Administration
is licensed under a
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Site updated April 30, 2024
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