Full-Time

Clinical Research Coordinator 1

University of Miami

University of Miami

Research university in Coral Gables, FL

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA + 1 more

More locations: New York, NY, USA

Hybrid

Hybrid work is available with fieldwork in either Miami or New York City; the schedule may include weekends.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Data Analysis

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Requirements
  • A Bachelor's degree in a relevant field is required.
  • A minimum of 1 year of relevant experience is required.
  • A strong background in neuroscience or psychology with previous research experience is required.
  • The ability to complete assignments accurately and with attention to detail is required.
  • The ability to analyze, organize, and prioritize work under pressure while meeting deadlines is required.
  • The ability to process and handle confidential information with discretion is required.
  • The ability to work evenings, nights, and weekends as necessary is required.
  • The ability to work independently and/or in a collaborative environment is required.
Responsibilities
  • Perform chart review and pre-screening activities for study participant eligibility and coordinate simple clinical research protocols while maintaining 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, including those 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 applicable international, national, and local regulatory bodies.
  • Maintain knowledge of and 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.
  • Conduct research studies and related projects.
  • Perform research participant-related activities, including recruitment, screening, psychiatric assessment, data collection, analysis, and management using electronic data capture systems.
  • Interact with patients' treatment teams, conduct imaging acquisition, and prepare manuscripts.
  • Conduct studies according to protocol design, report deviations, and maintain study files including regulatory documents, correspondence, case report forms, and data files.
  • Perform regulatory-compliance activities such as Institutional Review Board submissions and mandates issued by the study sponsor or another regulatory entity.

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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