Full-Time

Clinical Research Coordinator 1

Posted on 5/9/2026

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (1)
Requirements
  • Bachelor’s degree in relevant field
  • Minimum 1 year of relevant experience
  • 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’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
  • Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility. Collects, processes, and ships specimens according to protocol and regulations. Maintains study binders and filings according to protocol requirements, UM, and department policy. Distribute study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator. Assists in implementing protocol amendments under direct supervision of the Principal Investigator. Assists with study orientation and protocol-related in-services to the research team and clinical staff. Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule. Learns the research team and assists with communications/interactions with sponsors, data coordinating centers, compliance monitors, collaborators, investigators’ academic, administrative personnel, and departments. Assists in administrative tasks of study personnel, including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews. Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc.
  • Supports bilingual communication when required; English and Spanish language skills preferred but not required
Desired Qualifications
  • Bilingual in English and Spanish is preferred but not required

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