University of Miami

University of Miami

Research university in Coral Gables, FL

Clinical Research Coordinator

Full-Time
No salary listed
Junior
Bachelor's
Miami, FL, USA
In Person
Company Does Not Provide H1B Sponsorship

About the job

Requirements
  • A bachelor's degree in a relevant field is required.
  • At least one year of relevant experience is required.
  • Complete assignments accurately and with attention to detail.
  • Analyze, organize, and prioritize work under pressure while meeting deadlines.
  • Process and handle confidential information with discretion.
  • Work evenings, nights, and weekends as necessary.
  • Work independently and/or in a collaborative environment.
Responsibilities
  • Conduct research studies and related projects.
  • Recruit, screen, and assess research participants, collect and analyze data, and manage data using electronic data capture systems.
  • Interact with patients' treatment teams and perform imaging acquisition.
  • Prepare manuscripts.
  • Conduct studies according to protocol design and report deviations as they arise.
  • Maintain study files, including regulatory documents, correspondence, case report forms, and data files.
  • Perform regulatory compliance activities, including institutional review board submissions and mandates issued by study sponsors or other regulatory entities.
  • Review charts and pre-screen participants for study eligibility and coordinate simple clinical research protocols.
  • Maintain enrollment procedures according to the protocol.
  • Coordinate routine clinical study activities, including data collection and maintenance, study timeline planning, appointment and study visit scheduling, meeting scheduling, and project evaluation.
  • Perform moderate to complex research tests and experiments and adapt procedures for quality improvement under supervision.
  • Follow technical instructions for operating clinical research equipment and troubleshoot operational failures.
  • Assist in observing and informing the principal investigator or supervisor of adverse events reported by study participants.
  • Address adverse events according to protocol while advocating for study participants and quality standards throughout the study.
  • Identify, report, and help resolve protocol deviations and unanticipated occurrences.
  • Follow the fundamental requirements of international, national, and local regulatory bodies.
  • Maintain study-specific clinical research regulatory binders.
  • Maintain 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.
Desired Qualifications
  • A strong background in neuroscience or psychology with previous research experience.

About the company

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

Company Size

N/A

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A

Get referred to University of Miami

See people who can refer or advise you