U

University of Miami

Research university in Coral Gables, FL

Clinical Research Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeMiami, FL, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in a relevant field or equivalent is required.
  • At least 1 year of relevant experience is required.
  • The role requires accurate completion of assignments with attention to detail.
  • The role requires the ability to analyze, organize, and prioritize work under pressure while meeting deadlines.
  • The role requires discretion when processing and handling confidential information.
  • The role requires the ability to work evenings, nights, and weekends as necessary.
  • The role requires the ability to work independently and in a collaborative environment.
  • The role requires flexibility to travel to all Bascom Palmer Eye Institute sites as needed.
  • The role requires the ability to handle multiple clinical trials with several principal investigators.

Responsibilities

  • Perform chart review and participant eligibility prescreening and coordinate simple clinical research protocols.
  • Maintain enrollment procedures according to study protocols.
  • Coordinate routine clinical study activities, including data collection and maintenance, study timelines, appointments, study visits, meetings, and project evaluation.
  • Perform moderate to complex research tests and experiments and adapt procedures for quality improvement under supervision.
  • Operate clinical research equipment according to technical instructions and troubleshoot operational failures.
  • Observe and inform the principal investigator or supervisor of participant-reported and other adverse events.
  • Address adverse events according to protocol while advocating for study participants and quality standards.
  • Identify, report, and help resolve protocol deviations and unanticipated occurrences.
  • Follow the requirements of international, national, and local regulatory bodies.
  • Maintain study-specific clinical research regulatory binders.
  • Maintain required skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Adhere to University and unit-level policies and procedures and safeguard University assets.
  • Establish participant screening procedures with the principal investigator and obtain relevant medical information from clinic charts and medical records.
  • Serve as a backup coordinator for other clinical trials.
  • Complete audit and monitor-visit corrections and queries and take action to correct deviations.
  • Maintain contact with patients or participants, healthcare providers, community agencies, and study sponsors.
  • Update sponsors, the Institutional Review Board, and other appropriate agencies on the current status of research projects.
  • Provide in-service education to staff and patients or participants about research protocols.
  • Prepare and submit annual reviews to the Institutional Review Board.
  • Maintain consent forms and sponsor correspondence.
  • Notify the Institutional Review Board of protocol amendments, safety reports, and serious adverse events in compliance with applicable regulations.
  • Implement research protocols and monitor participant adherence to protocols.

About the Company

University of Miami

Research university in Coral Gables, FL

The University of Miami is a private research university focused on education, discovery, and service, with undergraduate, graduate, and professional programs.

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