Clinical Research Coordinators

A typical week, in the words of people in the job

1. 01Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
2. 02Direct the requisition, collection, labeling, storage, or shipment of specimens.
3. 03Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
4. 04Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
5. 05Code, evaluate, or interpret collected study data.
6. 06Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
7. 07Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
8. 08Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
9. 09Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
10. 10Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
11. 11Inform patients or caregivers about study aspects and outcomes to be expected.
12. 12Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.

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