×
Register Here to Apply for Jobs or Post Jobs. X

OPS Clinical Research Coordinator - Vascular Surgery

Job in Gainesville, Alachua County, Florida, 32635, USA
Listing for: University Of Florida
Full Time, Seasonal/Temporary position
Listed on 2026-07-31
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 23.5 USD Hourly USD 23.50 HOUR
Job Description & How to Apply Below

OPS Clinical Research Coordinator - Vascular Surgery

Job no: 540724
Work type: Temp Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Office/Administrative/Fiscal Support, Health Care Administration/Support
Department:  - MD-SURGERY-VASCULAR

Classification

Title:

OPS Clinical Research Coordinator

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

Job Description:

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, preclinicalstudies, and clinical protocols. Helps with protocol development and protocol endpoints to ensure statistical and clinical relevance ofstudies. 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 asneeded for preclinical studies within Division.

Assists with manuscript preparation and abstract submission for principal investigators.

Submits protocols to the RAC and IRB offices to assure compliance under the direction of the senior study coordinator. Organizes and maintains regulatory files for clinical studies performed within Division.

Interacts with institutional Investigational Review Board under direction of Principal Investigator for clinical research protocols.

Tracks the type of study services performed to ensure that they are compensated appropriately.
Performs billing review for study subjects.
Dispense human subjects’ payments to study participants

$23.50 per hour

Required Qualifications:

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; must be able to communicate with patients and family participating in clinical trials.

Experience as research coordinator preferred.

Experience with patient data and/or databases.

Proficient time management skills and ability to successfully manage multiple studies.

Health Assessment

Required:

Health Assessment

Required:

Yes

Advertised: 24 Jul 2026 Eastern Daylight Time
Applications close: 31 Jul 2026 Eastern Daylight Time

The University of Florida is an Equal Employment Opportunity Employer.

We will email you new jobs that match this search.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary