Clinical Research Coordinator II

2 days ago

Jacksonville, Florida, United States University of Florida Full time $50,000 - $60,000 per year

JOB NO:

537629

WORK TYPE:

Staff Full-Time

LOCATION:

Jacksonville Campus

CATEGORIES:

Grant or Research Administration, Health Care Administration/Support

DEPARTMENT:

JX-DEAN-ADMINISTRATION

CLASSIFICATION TITLE:

Clinical Research Coordinator II

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:

Work independently and proactively to coordinate all necessary activities required to set up and

monitor a study, completing accurate study status reports and maintaining study documentation.

Submission of protocol, consent documents for IRB approval and assist in preparing regulatory

submissions as requested

Work at UF research locations prescreening, consenting and enrolling participants in research studies

Conduct study visits and follow ups including functions necessary for successful completion of all

protocol required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of

investigational product, scheduling, drug accountability/reconciliation and organizational tasks as needed.

Help Investigators with proposal development, progress reports, budget creation, regulatory

paperwork and study files.

Other duties as assigned by CRO/ORA leadership

EXPECTED SALARY:

$50,000 - $60,000 per year.

REQUIRED QUALIFICATIONS:

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

A Valid Driver's license is required.

PREFERRED:

Master's degree or an allied health professional degree in an appropriate area and one year of relevant

experience; or an equivalent combination of education and experience.

Experience in phlebotomy and clinical research is preferred.

Excellent interpersonal skills and the ability to prioritize and effectively communicate verbally and in writing.

Coordinates multiple tasks and work independently and productively in a fast paced, deadline-oriented

environment.

This position necessitates proficiency in data management and superior organization skills.

Integrity, careful attention to detail; ability to maintain confidentiality, demonstrate professionalism and

respect for subjects' rights and individual needs; willing to learn and maintain skills in accordance with

HIPAA regulations and Good Clinical Practice guidelines.

SPECIAL INSTRUCTIONS TO APPLICANTS:

In order to be considered, you must upload your cover letter and resume.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

HEALTH ASSESSMENT REQUIRED:

Yes

ADVERTISED:

29 Oct 2025

Eastern Daylight Time

APPLICATIONS CLOSE:

12 Nov 2025

Eastern Standard Time

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