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Clinical Research Coordinator, Entry Level
USF Health. Provide direct support to the lead coordinator or lead simple-to-moderate site-level projects .
Posted 11/5/2026full-timeTampa • Florida • United StatesMid-LevelSenior💰 $53,000 - $62,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting clinical assessments, coordinating clinical trial activities, and ensuring compliance with research protocols and regulations. Proficient in managing study participant interactions and maintaining accurate site documentation.
Highest-signal resume keywords
Clinical AssessmentsStudy Protocol ImplementationPatient Screening and EnrollmentCompliance MonitoringCommunication and Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
PhlebotomySample ProcessingVital Signs MeasurementECG AdministrationResearch Data Collection
Soft Skills
Guidance to StaffCollaborationCommunication
Tools & Technologies
Site Study DocumentsInventory Management Systems
Industry Keywords
Clinical TrialsSOPsHIPAARegulatory ComplianceClinical Research
About the role
Key responsibilities & impact- Provide direct support to the lead coordinator or lead simple-to-moderate site-level projects
- Perform patient clinical assessments for clinical trial visits and coordinate scheduling with vendors, departments, and outside facilities
- Screen, enroll, and retain study participants
- Conduct study visits and collect research data
- Implement assigned study protocol procedures and activities
- Communicate and collaborate with study and clinical teams
- Prepare and submit site study documents
- Assist with site monitoring visits, audits, and inspections
- Maintain site inventory and follow up with vendors, including lab and medical record retrieval
- Monitor study activity for compliance with protocols, SOPs, HIPAA, and applicable regulations
- Provide guidance to less experienced site staff
Requirements
What you’ll need- Bachelor's degree in a related field OR equivalent combination of education and experience
- Employment eligibility in the U.S.
- Related work experience may not substitute for required licensure, certification, or registration, where applicable
- Ability to perform delegated clinical assessments, including phlebotomy, sample processing, vitals, and ECGs, per assigned protocols
- Knowledge of clinical research protocols, site SOPs, applicable regulations, and HIPAA
Benefits
Comp & perks- Medical insurance
- Dental insurance
- Life insurance
- Retirement plan options
- Employee and dependent tuition programs
- Generous leave
- Employee perks and discounts