Full-Time

Clinical Research Coordinator 1

Posted on 11/23/2025

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (2)
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Requirements
  • Bachelor’s degree in a relevant field such as Public Health, Nutrition Science, Exercise Physiology or Kinesiology, Nursing Science, Health Promotion, etc.
  • Minimum 1 year of relevant experience in research
  • CCRC, CCRP, or CCRA certification preferred
  • Skill in completing assignments accurately and with attention to detail
  • Ability to analyze, organize and prioritize work under pressure while meeting deadlines
  • Ability to process and handle confidential information with discretion
  • Ability to work evenings, nights, and weekends as necessary
  • Commitment to the University of Miami’s core values
  • Ability to work independently and/or in a collaborative environment
Responsibilities
  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols
  • Maintains enrollment procedures according to the protocol
  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation
  • Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision
  • Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur
  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants
  • Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study
  • Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies. Knows the contents and maintenance of study-specific clinical research regulatory binders
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies
  • Adheres to University and unit-level policies and procedures and safeguards University assets

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INACTIVE