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TASK
Clinical Research Coordinators
ID
work_management/clinical_research_coordinators
Type
TASK
Children
33
Child Nodes (33)
ATOMIC
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
ATOMIC
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
ATOMIC
Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
ATOMIC
Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
ATOMIC
Inform patients or caregivers about study aspects and outcomes to be expected.
ATOMIC
Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
ATOMIC
Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
ATOMIC
Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
ATOMIC
Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
ATOMIC
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
ATOMIC
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
ATOMIC
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
ATOMIC
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
ATOMIC
Code, evaluate, or interpret collected study data.
ATOMIC
Direct the requisition, collection, labeling, storage, or shipment of specimens.
ATOMIC
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
ATOMIC
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
ATOMIC
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
ATOMIC
Order drugs or devices necessary for study completion.
ATOMIC
Contact outside health care providers and communicate with subjects to obtain follow-up information.
ATOMIC
Participate in the development of study protocols including guidelines for administration or data collection procedures.
ATOMIC
Confer with health care professionals to determine the best recruitment practices for studies.
ATOMIC
Communicate with laboratories or investigators regarding laboratory findings.
ATOMIC
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
ATOMIC
Organize space for study equipment and supplies.
ATOMIC
Develop advertising and other informational materials to be used in subject recruitment.
ATOMIC
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
ATOMIC
Arrange for research study sites and determine staff or equipment availability.
ATOMIC
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
ATOMIC
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
ATOMIC
Register protocol patients with appropriate statistical centers as required.
ATOMIC
Solicit industry-sponsored trials through contacts and professional organizations.
ATOMIC