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Research Regulatory Coordinator
Carle HealthSpecialized research professional coordinating regulatory aspects of clinical trials at Carle Health. Responsible for compliance with regulatory guidelines and documents for clinical research.
Posted 7/29/2026full-timeUrbana • Illinois • 🇺🇸 United StatesMid-LevelSenior💰 $26 - $43 per hourWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in regulatory compliance, including the preparation and submission of required documents, informed consent review, and maintenance of regulatory databases. Proficient in training staff on regulatory processes and managing electronic filing systems for industry-sponsored research.
Highest-signal resume keywords
Certified Clinical Research Professional (CCRP)Regulatory ComplianceInformed Consent ReviewRegulatory Document ManagementStaff Training
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Regulatory Document PreparationConsent Form ModificationProtocol Information ManagementStudy Approval TrackingElectronic Filing Management
Soft Skills
Attention to DetailOrganizational SkillsCommunication Skills
Tools & Technologies
Regulatory Database
Certifications & Qualifications
Certified Clinical Research Professional (CCRP)
Industry Keywords
Regulatory ComplianceIndustry-Sponsored ResearchAudit PreparationExternal Sponsor Visits
About the role
Key responsibilities & impact- Prepares, completes, and submits required forms and documents for regulatory compliance
- Performs Informed Consent review and modifies consent forms
- Ensures consent language matches contracts and protocol
- Completes and maintains regulatory documents for industry-sponsored research
- Prepares for and participates in audits and external sponsor visits
- Updates and maintains current protocol information on the Research website
- Tracks study approvals and expirations
- Maintains regulatory database and manages electronic filing of documents
- Trains staff on regulatory processes
Requirements
What you’ll need- Certified Clinical Research Professional (CCRP) within 3 years
- Bachelor's Degree in Related Field or experience in lieu of education
- Related field work experience
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development opportunities