Clinical Research Coordinator II-Peds ID

University of Florida; Gainesville (FL); On-site; USD 59,000 - 67,000; Full time

Job summary

University of Florida Jacksonville campus seeks a Clinical Research Coordinator II-Peds ID to independently manage assigned clinical research studies under UF CARES, including HIV-related and infectious disease protocols involving pediatric, adolescent, and adult participants.

The role covers participant identification, consent, study visits, data management, regulatory compliance, and collaboration with investigators and sponsors. Requires a Bachelor's degree and two years of related experience.

Qualifications

• Requires Bachelor's degree in an appropriate area and two years of relevant experience or an equivalent combination of education and experience.
• Experience coordinating clinical research studies, including HIV/AIDS or infectious disease research, is preferred.

Responsibilities

• Coordinate and implement assigned clinical research studies in accordance with study protocols and GCP.
• Identify, recruit, screen, enroll, and retain participants; manage informed consent and assent.
• Coordinate study visits, procedures, data collection, and regulatory requirements; communicate with investigators, sponsors, and study teams.

Education

Bachelor's degree in an appropriate area

Job description

Clinical Research Coordinator II-Peds ID

Job No: 541314

Work Type: Full Time

Location: Jacksonville Campus

Categories: Allied Health, Office/Administrative/Fiscal Support, Grant or Research Administration, Health Care Administration/Support

Department: 30090000 - JX-PEDIATRICS-JACKSONVILLE

Job Description

Classification Title: Clinical Research Coordinator II-Peds ID

Classification Minimum Requirements: Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

Job Description: Responsible for advanced-level coordination and implementation of assigned clinical research studies conducted through UF CARES, including HIV-related and other infectious disease research involving pediatric, adolescent, and adult participants. Independently coordinates assigned treatment, observational, and data/chart-based research studies in accordance with study protocols, institutional policies, Good Clinical Practice (GCP), and applicable federal and regulatory requirements. Coordinates research activities throughout the study lifecycle, including participant identification, recruitment and retention; informed consent and assent; study visits and procedures; collection and management of research data; specimen collection and processing; adverse event and protocol deviation reporting; regulatory compliance; and communication with investigators, sponsors, study teams, and other stakeholders.

Participant Recruitment, Screening, Enrollment & Retention: Identifies, recruits, and screens potential research participants according to protocol specific eligibility criteria. Coordinates and conducts the informed consent and assent process using current IRB-approved documents and ensures appropriate documentation in the research record and Epic, as applicable. Maintains ongoing communication with participants and families to support study participation, retention, adherence to protocol requirements, and continuity of care.

Study Coordination & Protocol Implementation: Coordinates assigned clinical research protocols from study activation through participant follow-up and study closeout activities, as applicable. Plans and coordinates study visits, assessments, procedures, medication dispensing, laboratory testing, and other protocol-required activities. Develops and maintains protocol specific worksheets, source documents, tracking tools, and other materials necessary for effective study implementation. Cross-trains on additional studies and provides coverage for other research coordinators as assigned.

Research Data Collection, Documentation & Quality Assurance: Collects, reviews, enters, and maintains clinical research data obtained from medical records, participant interviews, questionnaires, laboratory results, and other approved sources. Completes and submits Case Report Forms (CRFs) and other study documentation accurately and within required timelines. Reviews data for accuracy, completeness, and consistency and promptly resolves data queries, logic checks, errors, and delinquencies. Participates in research quality assurance activities and supports monitoring, auditing, and data validation activities.

Regulatory Compliance & Participant Safety: Maintains knowledge of and compliance with applicable research regulations, institutional policies, IRB requirements, FDA requirements, Good Clinical Practice, sponsor requirements, and protocol-specific procedures. Identifies, documents, and communicates protocol deviations, adverse events, serious adverse events, toxicities, abnormal laboratory findings, and other reportable events according to applicable requirements and established timelines. Completes laboratory toxicity grading using the DAIDS toxicity table or other protocol-specific grading criteria when applicable.

Clinical Research Procedures & Specimen Management: Performs protocol‑required phlebotomy for pediatric and/or adult research participants within demonstrated competency and scope of responsibility. Processes, prepares, labels, stores, tracks, and ships research specimens according to protocol, laboratory, and regulatory requirements. Performs centrifuging and aliquoting and assists with research specimen storage and freezer monitoring/maintenance. Ensures required study laboratory tests and diagnostic procedures are completed, reviewed, and appropriately documented.

Research Team, Investigator & Sponsor Communication: Communicates and collaborates with investigators, healthcare providers, research participants and families, research pharmacists, protocol teams, sponsors, monitors, IRB personnel, laboratories, and UF CARES staff regarding study activities and participant needs. Communicates relevant clinical and research information, including signs and symptoms, toxicities, abnormal results, protocol deviations, adverse events, and study requirements, to appropriate members of the research and clinical teams. Serves as a knowledgeable resource regarding assigned protocols and research procedures.

Research Education & Team Support: Provides protocol-specific education and in‑services to UF CARES staff and other participating personnel as appropriate. Maintains current knowledge of assigned clinical research areas through protocol training, required continuing education, investigator meetings, study activities, and review of relevant research literature. Serves as a cross‑trained resource and backup for other clinical research staff and assists with onboarding and training activities as assigned.

Research Billing & Administrative Coordination: Supports accurate research billing and financial documentation related to assigned studies. Maintains required study visit and billing documentation, completes applicable research referral or billing forms, and works with appropriate research and administrative personnel to ensure study‑related services and charges are appropriately identified and documented.

Background Check is Required.

University of Florida College of Medicine – Jacksonville: Visit this link to watch the video.

University of Florida is a public institution and subject to all requirements under the Florida Sunshine and Public Records laws. If an accommodation due to a disability is needed to apply for this position, please call (352) 392-2HRS or the Florida Relay System at [phone] (TDD). Hiring is contingent upon eligibility to work in the U.S. Searches are conducted in accordance with Florida's Sunshine Law. Health Assessment Required: yes

Expected Salary

$59,000-$67,000

Required Qualifications

Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

Preferred Qualifications

Bachelor's Degree in Nursing with current Florida licensure and clinical research experience; master's degree in an appropriate area of specialization; or a bachelor's degree in an appropriate area of specialization with relevant clinical research experience. Two or more years of experience coordinating clinical research studies, preferably involving HIV/AIDS, or infectious diseases. Clinical research certification (e.g., CCRC, CCRP, or equivalent) preferred or ability to obtain certification within two years of hire.

Applications Close

30 September 2026

Our Commitment

The University of Florida is an Equal Employment Opportunity Employer.

Hiring is contingent on eligibility to work in the U.S. The University of Florida is a public institution and is subject to all requirements under the Florida Sunshine and Public Records laws. If an accommodation due to a disability is needed to apply for this position, please call 352-392-2477 or the Florida Relay System at 800-955-8771 (TDD) or visit Accessibility at UF.