Clinical Research Assistant at Gastro Florida Clearwater, FL

Gastro Florida

Clearwater, FLFull-timePosted Apr 27, 2026

Behavioral Health Market Context

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Qualifications

  • •Gastroenterology
  • •High school or equivalent (Required)
  • •Clinical Research Associates & Coordinators: 1 year (Required)
  • •Willingness to travel:
  • •75% (Required)
  • •Criminal background and drug screening required as well as excellent professional references
  • •3 more items(s)

Responsibilities

  • •This individual will support the clinical research coordinators at various sites in the Tampa Bay region
  • •They will work under the direction of the Clinical Research Manager
  • •The candidate will receive training from the sponsors on the data systems
  • •Clinical Coordinator
  • •Evaluates potential research participants with Principal Investigator and randomizes participants into appropriate research study
  • •Consents patient for study enrollment
  • •Coordinates and schedules study visits and follow-ups
  • •Performs or coordinates tests and procedures as necessary (within certified scope of practice) and documents per study protocols
  • •May perform phlebotomy service
  • •Ensures data on each study participant for each visit is provided according to research protocol, maintaining complete study progress notes and case report form for each visit
  • •Prepares protocol applications, amendments and annual reviews and study sponsor communications to IRB as required
  • •Ensures that designated space/sites are certified for research per study requirements
  • •Coordinates ancillary clinical services not offered within the study site, including outside of the practice (e.g. radiology)
  • •Collects, analyzes, and performs quality assurance of study data
  • •Monitors overall clinical study to insure that quality control measures are in compliance with protocol
  • •Maintains documentation and communication to effectively facilitate study monitor visits
  • •Reports any adverse events according to the study protocol
  • •Actively meets with investigators to discuss study progress/status
  • •Ensure that monthly quarterly, annual and end of grant reports are completed and submitted to regulatory and granting agencies as required
  • •Provides Administration updates on enrollment, financial, and other performance metrics
  • •17 more items(s)
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