Clinical Research Coordinator

USF Health

. Plan, organize, and manage resources necessary to achieve clinical research project goals and objectives at a single site .

Posted 9/18/2026contractRemote • Florida • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research projects, ensuring compliance with protocols, and performing clinical assessments. Proficient in data management and communication with stakeholders to facilitate successful trial execution.

Highest-signal resume keywords

Clinical Research Project ManagementPatient Clinical AssessmentsProtocol ComplianceData Entry and Query ResolutionCase Report Form Review

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PhlebotomySample ProcessingVital Signs MonitoringElectrocardiograms (ECGs)Clinical Trial ProtocolsSource Document CompletionDatabase ManagementClinical Research Documentation

Soft Skills

CommunicationTeam CollaborationGuidance and Support

Tools & Technologies

Research Project DatabasesFlowsheets

Certifications & Qualifications

Level II Background Check

Industry Keywords

Clinical TrialsStudy SponsorsThird-Party VendorsCompliance Standards

About the role

Key responsibilities & impact

Plan, organize, and manage resources necessary to achieve clinical research project goals and objectives at a single site
Coordinate and perform patient clinical assessments for clinical trial visits, including scheduling with vendors and other departments or outside facilities
Perform delegated clinical assessments such as phlebotomy, sample processing, vitals, and ECGs according to assigned protocols
Communicate with study sponsors, third-party vendors, clinical teams, and patients to ensure protocol requirements are completed within defined windows
Ensure site compliance with research protocols
Review case report forms and audit accuracy against source documents
Attend site monitoring meetings with sponsors
Manage site research project databases and develop flowsheets and other study-related documents
Complete source documents and case report forms
Provide guidance to clinical research staff and support personnel as needed
Recommend procedures to facilitate protocol compliance
Perform data entry and query resolution throughout assigned trials
Serve as a resource for internal and external customers and community members regarding clinical research processes

Requirements

What you’ll need

Bachelor's degree in a related field OR equivalent combination of education and experience
Minimum of two (2) years of related experience preferred
Level II background check required
Must meet all employment eligibility requirements in the U.S.

Benefits

Comp & perks

Medical, dental, and life insurance plans
Retirement plan options
Employee and dependent tuition programs
Generous leave
Hundreds of employee perks and discounts