Entry-Level Clinical Research Coordinator - On-Site, Miami

University of Miami

Miami (FL)

Hybrid

USD 60,000 - 75,000

Full time

7 days ago
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Benefits offered by this job

Restaurant d'entreprise
Indemnités de stage/alternance

Job summary

The University of Miami is seeking a Clinical Research Coordinator 1 to support the Clinical Translational Research Site in Miami. This entry-level role handles data management, protocol implementation, and coordination of study activities under supervision.

You will perform chart reviews, assist with IRB submissions, collect and verify study data, and ensure regulatory documents are up to date. Strong attention to detail and the ability to work evenings or weekends as needed are valued.

Qualifications

  • 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.

Responsibilities

  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
  • 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.
  • 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.
  • Maintains inspection-ready records for assigned tasks and completes remediation before independent performance when competency has not been demonstrated.
  • Demonstrates learning agility, reliability, professional communication, teamwork, time management, and responsiveness to coaching.
  • Participates in onboarding, shadowing, direct observation, mock exercises, and competency reassessment; seeks assistance before acting outside training or delegation.
  • Travel across different locations if necessary

Skills

Attention to detail
Data organization
Discretion with confidential info
Time management
Evenings/nights/weekends flexibility

Education

Bachelor's degree in relevant field

Job description

The University of Miami is seeking a Clinical Research Coordinator 1 to support the Clinical Translational Research Site in Miami. This entry-level role handles data management, protocol implementation, and coordination of study activities under supervision.

You will perform chart reviews, assist with IRB submissions, collect and verify study data, and ensure regulatory documents are up to date. Strong attention to detail and the ability to work evenings or weekends as needed are valued.

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