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Job Details

Employment Type

Full time

Salary

53,655.00 USD

Valid Through

Aug 24, 2025

Job Description

Apply now Job no: 536554Work type: Staff Full-TimeLocation: Jacksonville CampusCategories: Biology/Life Science, Allied Health, Grant or Research AdministrationDepartment: 30010100 - JX-DEAN-ADMINISTRATIONClassification TitleClinical Research Coordinator IIJob DescriptionWork independently and proactively to coordinate all necessary activities required to set up andmonitor a study, completing accurate study status reports and maintaining study documentation.

Submission of protocol, consent documents for IRB approval and assist in preparing regulatorysubmissions as requestedWork at UF research locations prescreening, consenting and enrolling participants in research studiesConduct study visits and follow ups including functions necessary for successful completion of allprotocol required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing ofinvestigational product, scheduling, drug accountability/reconciliation and organizational tasks as needed. Help Investigators with proposal development, progress reports, budget creation, regulatorypaperwork and study files. Other duties as assigned by CRO/ORA leadershipExpected Salary$50,000- $60,000 per year.

Minimum RequirementsBachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience. Preferred QualificationsMasters degree or an allied health professional degree in an appropriate area and one year of relevantexperience; 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-orientedenvironment. This position necessitates proficiency in data management and superior organization skills.

Integrity, careful attention to detail; ability to maintain confidentiality, demonstrate professionalism andrespect for subjects’ rights and individual needs; willing to learn and maintain skills in accordance withHIPAA regulations and Good Clinical Practice guidelines. Special Instructions To ApplicantsIn 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. This is a time-limited position. Health Assessment Required: YesAdvertised: 24 Jul 2025 Eastern Daylight TimeApplications close: 07 Aug 2025 Eastern Daylight TimeBack to search results Apply nowRefer a friendWhatsapp Facebook LinkedIn Email App

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