Clinical Research Coordinator I jobs in United States
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University of South Florida Libraries · 12 hours ago

Clinical Research Coordinator I

The University of South Florida Libraries is seeking a Clinical Research Coordinator I to manage clinical research studies. The role involves coordinating participant recruitment, conducting study visits, and ensuring compliance with regulatory standards.

Higher Education

Responsibilities

Coordinate a portfolio of clinical research studies under the supervision of the Principal Investigator (PI)
Recruit and screen participants; obtain initial and ongoing informed consent from participants and families
Provide research-related services and interventions per study protocol
Schedule and conduct study visits and follow-ups within protocol-defined visit windows
Administer investigational products and perform protocol-defined procedures, such as: Vital signs and anthropometric measurements, Phlebotom, Electrocardiograms (ECGs), Injections and other clinical assessments as delegated and based on training/experience, Communicate participant progress and safety updates to Investigators
Assist with the daily operations and coordination of CRC activities across multiple research studies and users
Support the development, documentation, and dissemination of CRC policies, procedures, and standard operating procedures (SOPs)
Ensure adherence to quality assurance and regulatory compliance standards
Serve as a liaison between CRC and internal/external stakeholders including investigators, research staff, USF Health Care providers, volunteers, sponsors, and Contract Research Organizations (CROs)
Collect, process, and ship biological samples per study requirements
Maintain biohazardous material shipping certification and comply with all infection control and safety standards
Track and manage investigational product accountability and study supplies
Coordinate with Investigational Pharmacies and partner institutions when applicable
Fulfill registration or certification requirements for research activities conducted at affiliate sites
Perform other related duties as assigned to support research goals and institutional mission

Qualification

Clinical trial coordinationGCP guidelinesICH guidelinesHuman subjects protections trainingPhlebotomy experienceTrainingMicrosoft Office proficiencyMedical terminologyInfection control knowledgeSoft skills

Required

Bachelor's degree
Four years of direct experience for a bachelor's degree
Senate Bill 1310- The Florida Senate is conditional upon meeting all employment eligibility requirements in the U.S
Related work experience may not substitute for any required licensure, certification, or registration required for the position of employment as established by the public employer and indicated in the advertised description of the position of employment
Minimum Qualifications that require a high school diploma are exempt from SB 1310

Preferred

Human subjects protections training
Knowledge of the Code of Federal Regulations
GCP (Global Good Clinical Practice)
ICH (International Council for Harmonization) Guidelines as applied to clinical trials
IRB and other regulatory processes and procedures including HIPAA
Shipping biohazard materials certification preferred
Current certification in clinical research is preferred
Strong working knowledge in Microsoft Office programs and other software packages
Medical and research terminology, processes and procedures
Phlebotomy experience
ECG training and training in other clinical procedures
General knowledge of infection control procedures

Benefits

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

Company

University of South Florida Libraries

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The University of South Florida Libraries accelerate learning and knowledge production through distinctive collections, information service innovation, and thought leadership.

Funding

Current Stage
Growth Stage
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