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.
Time card
| Mine | Task, by time spent | Human | With AI | AI | Robot |
|---|---|---|---|---|---|
| Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.54m a shift · No AI or robot evidence found | |||||
| Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.42m a shift · No AI or robot evidence found | |||||
| Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.42m a shift · No AI or robot evidence found | |||||
| Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.30m a shift · No AI or robot evidence found | |||||
| Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.24m a shift · No AI or robot evidence found | |||||
| Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.24m a shift · No AI or robot evidence found | |||||
| Oversee subject enrollment to ensure that informed consent is properly obtained and documented.24m a shift · No AI or robot evidence found | |||||
| Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.24m a shift · No AI or robot evidence found | |||||
| Inform patients or caregivers about study aspects and outcomes to be expected.18m a shift · No AI or robot evidence found | |||||
| Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.18m a shift · No AI or robot evidence found | |||||
| Direct the requisition, collection, labeling, storage, or shipment of specimens.18m a shift · Robots only in factory cells | |||||
| Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.12m a shift · No AI or robot evidence found | |||||
| Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.12m a shift · No AI or robot evidence found | |||||
| Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.12m a shift · No AI or robot evidence found | |||||
| Code, evaluate, or interpret collected study data.12m a shift · Observed in AI useTypical AI request: about 6h 54m alone, 1h 1m with AI | |||||
| Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.12m a shift · No AI or robot evidence found | |||||
| Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.12m a shift · No AI or robot evidence found | |||||
| Communicate with laboratories or investigators regarding laboratory findings.12m a shift · No AI or robot evidence found | |||||
| Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.6m a shift · No AI or robot evidence found | |||||
| Order drugs or devices necessary for study completion.6m a shift · No AI or robot evidence found | |||||
| Contact outside health care providers and communicate with subjects to obtain follow-up information.6m a shift · No AI or robot evidence found | |||||
| Participate in the development of study protocols including guidelines for administration or data collection procedures.6m a shift · No AI or robot evidence found | |||||
| Confer with health care professionals to determine the best recruitment practices for studies.6m a shift · No AI or robot evidence found | |||||
| Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.6m a shift · No AI or robot evidence found | |||||
| Organize space for study equipment and supplies.6m a shift · Robots only in factory cells | |||||
| Develop advertising and other informational materials to be used in subject recruitment.6m a shift · No AI or robot evidence found | |||||
| Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.6m a shift · Robots only in factory cells | |||||
| Arrange for research study sites and determine staff or equipment availability.6m a shift · No AI or robot evidence found | |||||
| Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.6m a shift · No AI or robot evidence found | |||||
| Register protocol patients with appropriate statistical centers as required.6m a shift · No AI or robot evidence found | |||||
| Participate in preparation and management of research budgets and monetary disbursements.6m a shift · No AI or robot evidence found | |||||
| Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.time not estimated · No AI or robot evidence found | |||||
| Solicit industry-sponsored trials through contacts and professional organizations.time not estimated · No AI or robot evidence found |
