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Clinical Research Coordinator - Vascular Surgery

Job in Gainesville, Alachua County, Florida, 32635, USA
Listing for: University of Florida
Full Time position
Listed on 2026-07-20
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 46000 - 50000 USD Yearly USD 46000.00 50000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Coordinator I - Vascular Surgery

Overview

Clinical Research Coordinator I - Vascular Surgery — Full Time.

Location:

Main Campus (Gainesville, FL). Job No: 540601. Department:  - MD-SURGERY-VASCULAR. Categories:
Grant or Research Administration, Health Care Administration/Support.

Job Description

Clinical Research Coordinator I coordinates ongoing clinical research trials within the Division of Vascular Surgery under the direction of the senior study coordinator. As part of an interdisciplinary health team, the incumbent will collaborate with other Clinical Research Coordinators, physicians, nurses, and other key personnel in the department and clinic to ensure compliance with protocol requirements and satisfactory care for enrolled patients.

The incumbent will also assist in the development of protocol methodologies and data collection.

Responsibilities
  • Coordination of Protocol Subjects & Data Collection
  • Performs subject screening and consent for clinical protocols under direction of Principal Investigator.
  • Serves as patient resource and educator for information regarding the study or clinical symptoms.
  • Prepares and ships central laboratory samples as per protocol requirements.
  • Collects baseline and follow-up data from the medical record.
  • Documents findings in appropriate source records and case report forms.
  • Schedules and attends clinic appointments for patients as required by protocol.
  • Communicates with nursing staff and OR staff about patient care according to protocols.
  • Assists with operating room protocol requirements where appropriate.
  • Records patient symptoms and adverse events in conjunction with care providers.
  • Reports and follows up adverse events and serious adverse events, after discussion with Principal Investigator, to sponsor and Investigational Review Board as required by protocol.
  • Coordination of Protocol Compliance
  • Maintains knowledge base of Good Clinical Practice Guidelines and Federal Code of Regulations regarding clinical trial conduct.
  • Coordinates and maintains HIPAA compliance for assigned studies.
  • Communicates with interdisciplinary health team in care of patients involved in research studies to ensure regulatory compliance.
  • Interacts with local laboratories and diagnostic study centers to ensure clinical protocol requirements are complete for studies.
  • Coordinates efforts of Investigational Pharmacist and maintains site records for Good Clinical Practice and sponsor guidelines.
  • Research Support
  • Assists medical and scientific partners to design protocol methodologies for basic science, preclinical studies, and clinical protocols.
  • Helps with protocol development and protocol endpoints to ensure statistical and clinical relevance of studies.
  • Assesses clinical needs by performing literature review and discussion with faculty advisors within Division.
  • Prepares and submits filings of protocols to Investigational Review Board and Animal Care Committees as needed.
  • Designs Case Report Forms and Source Documents for clinical protocols where required.
  • Assists with grant development projects. Maintains awareness of Good Laboratory Practices as needed.
Qualifications
  • Required: Associate’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.
  • Preferred: Excellent communication skills; ability to communicate with patients and families participating in clinical trials. Experience as a research coordinator preferred. Experience with patient data and/or databases. Proficient time management skills and ability to manage multiple studies.
Expected Salary

$46,000 - $50,000

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.

Compliance & Accessibility

Health Assessment

Required:

Yes. Our Commitment:
The University of Florida is an Equal Employment Opportunity Employer. Hiring is contingent on eligibility to work in the U.S. UF is a public institution and is subject to Florida Sunshine and Public Records laws. If an accommodation due to a disability is needed to apply for this position, please call  or the Florida Relay System at  (TDD) or visit Accessibility at UF.

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