Clinical Research Coordinators
Management
Day to day you keep a clinical study on protocol. You screen people for eligibility through interviews, medical records, or talks with physicians and nurses, then schedule appointments, procedures, or hospital stays. You may interview subjects, take vital signs, or run electrocardiograms, and you explain the study and expected outcomes to patients or caregivers. Documentation is constant: worksheets, manuals, progress reports, informed consent, and adverse-event records that you discuss with investigators before they go to oversight agencies. Fits those who want careful follow-through, tidy records, and work with both patients and research staff under strict rules.
Typical education: Bachelor’s Degree (4-year)
Annual Median Wage in Field (2025)
$167'220
Median Wage Market Position
$167'220
What you might do
- Screen people who want to join the study
- Schedule visits, tests, and hospital stays
- Interview subjects and take their vital signs
- Explain the study and collect signed consent
- Draft protocol forms, reports, and board paperwork
- Log side effects and confirm the study follows rules
Skills that matter
- Reading protocols to screen subjects
- Listening during eligibility interviews
- Writing adverse event and progress reports
- Explaining expected outcomes to patients
- Monitoring studies for protocol compliance
- Supporting patients and caregivers through studies
AI & the future of this role
Software may take over protocol tracking, scheduling, and routine data checks, while participant consent, site coordination, and compliance judgment still matter. Prospects sit in a middle range as sponsors automate admin work but still need people who keep trials running on the ground.
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Includes O*NET® 30.3 Database information by USDOL/ETA under CC BY 4.0; modified by LostInCareer. Wage/outlook from BLS. Attribution details