ManagementO*NET: 11-9121.01
Will AI Replace Clinical Research Coordinators?
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.
36out of 100
Low Risk
AI Risk Score
36/100
Risk Level
Low
Job Zone
4/5
Advanced
Total Tasks Analyzed
26
🤖 What AI Can Do
- ▸Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
- ▸Assess 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.
- ▸Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
- ▸Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
- ▸Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
👤 What Requires Humans
- ▸Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
- ▸Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
Task Breakdown
🤖AI Can Automate (18)
- Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
- Assess 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.
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
- Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
- Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
- Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
- Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
- Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
- Code, evaluate, or interpret collected study data.
- Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
- Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
- Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
- Contact outside health care providers and communicate with subjects to obtain follow-up information.
- Participate in the development of study protocols including guidelines for administration or data collection procedures.
- Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
- Organize space for study equipment and supplies.
- Develop advertising and other informational materials to be used in subject recruitment.
👤Requires Humans (2)
- Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
- Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
⚡AI-Assisted (6)
- Inform patients or caregivers about study aspects and outcomes to be expected.
- Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
- Direct the requisition, collection, labeling, storage, or shipment of specimens.
- Order drugs or devices necessary for study completion.
- Confer with health care professionals to determine the best recruitment practices for studies.
- Communicate with laboratories or investigators regarding laboratory findings.
Key Skills Analysis
Reading ComprehensionAI-Vulnerable
Importance: 4.00/5.00
Active Listening
Importance: 4.00/5.00
WritingAI-Vulnerable
Importance: 4.00/5.00
Speaking
Importance: 3.88/5.00
CoordinationAI-Resistant
Importance: 3.88/5.00
Critical ThinkingAI-Resistant
Importance: 3.75/5.00
Monitoring
Importance: 3.62/5.00
Social PerceptivenessAI-Resistant
Importance: 3.62/5.00
Complex Problem SolvingAI-Resistant
Importance: 3.62/5.00
Judgment and Decision MakingAI-Resistant
Importance: 3.62/5.00
Time ManagementAI-Resistant
Importance: 3.50/5.00
Management of Personnel ResourcesAI-Resistant
Importance: 3.50/5.00
Active LearningAI-Resistant
Importance: 3.38/5.00
Learning Strategies
Importance: 3.12/5.00
InstructingAI-Resistant
Importance: 3.12/5.00
Related Occupations
Future-Proof Your Career
Whether AI poses a high or low risk to your role, staying ahead means continuous learning. Explore courses to build AI-resistant skills.
Frequently Asked Questions
Based on our analysis, Clinical Research Coordinators have a low risk of AI replacement with a score of 36/100. This role requires significant human skills like creativity, empathy, and complex decision-making that AI cannot easily replicate.
Last updated: 2026-03-28· Data from O*NET 30.2 & Frey/Osborne automation research