Clinical Research Associate

USF Health

. Report to the principal investigator of a clinical research study .

Posted 9/29/2026full-timeTampa • Florida • United StatesJuniorMid-Level💰 $52,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research coordination, including data quality control, regulatory compliance, and effective communication with clients and stakeholders. Proficient in managing study documents, budgets, and training clinical staff while ensuring adherence to federal and state regulations.

Highest-signal resume keywords

Clinical Research CoordinationData Quality ControlRegulatory ComplianceTraining DevelopmentSubstance Use Disorder Research

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data CollectionClinical Trial Data AnalysisBudget ManagementProtocol ImplementationRegulatory Document Preparation

Soft Skills

CommunicationCollaborationSupervisionProblem-Solving

Tools & Technologies

Electronic Health RecordsData Management SystemsWebsite Maintenance

Certifications & Qualifications

Bachelor's DegreeMaster's DegreeEmployment Eligibility in the U.S.

Industry Keywords

Behavioral HealthHealthcare OperationsInformed ConsentHIPAA ComplianceEmergency Medicine

About the role

Key responsibilities & impact

Report to the principal investigator of a clinical research study
Perform evaluation duties in preparation for projects
Oversee screening and enrollment of potential clients for health services protocols
Develop materials communicating projects to potential clients and their families
Coordinate site visits and appropriate data collection
Ensure data quality control and compile regulatory reports
Coordinate protocol implementation and collaborate with IT, pharmacy, nursing, physician groups, and administration
Facilitate clinical workflows and electronic health record order sets
Develop and deliver training for clinical staff
Supervise research personnel and recruit and train data-gathering assistants
Manage study documents and budgets and ensure project milestones are met
Monitor laboratory tests and referrals
Monitor compliance with federal, state, and university regulations
Maintain eligibility, informed consent, HIPAA, infection control, and safety documentation
Prepare and maintain regulatory and compliance documents such as IRB applications
Collect and analyze clinical trial or medical screening data and create client or medical-record databases
Collaborate with social workers and professional agencies
Disseminate study information to clients, families, and the general public
Draft program reports for publication or public dissemination
Perform other duties as assigned

Requirements

What you’ll need

Bachelor's degree in a field directly related to the program responsibilities and one year of professional experience; or Master's degree in an appropriate area of specialization
Employment eligibility requirements in the U.S.
Preferred experience in substance use disorder research, behavioral health, emergency medicine, clinical research, or healthcare operations
Position may require specific computer expertise
Position may require maintaining information on a website
Position may be subject to a Level 1 or Level 2 criminal background check

Benefits

Comp & perks

Medical insurance
Dental insurance
Life insurance
Retirement plan options
Employee and dependent tuition programs
Generous leave
Employee perks and discounts