UMiami
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Clinical Research Coordinator 1

Location
Miami, FL · On-site
Job type
Full-time
Level
Mid-level
Experience
1+ year
Education
Bachelor's degree
Listed
14 days ago

Skills & highlights for this role

  • Clinical research protocol coordination
  • Chart review and pre-screening
  • Data collection and maintenance
  • Adverse event reporting
  • Regulatory compliance
  • Attention to detail
  • Confidentiality management

Also useful

  • Clinical research equipment operation
  • Study timeline planning
  • Quality improvement
  • Collaborative teamwork

Current Employees

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.

About the role

The University of Miami/UHealth Hussman Institute has an exciting opportunity for a Full Time, Clinical Research Coordinator 1 to work in Miami.

Core Job Summary

The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties, and assumes responsibility for simple clinical research protocols and timelines.

Core 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.

Additional information

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

Core Qualifications

  • Bachelor’s degree in relevant field required
  • 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.

Pay and benefits

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

Job Status: Full time

Employee Type: Staff

Read the original posting

From UMiami's careers page, first listed on Rolev.ai on October 27, 2026. Rolev.ai is not the employer.

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Common questions

Where is the Clinical Research Coordinator 1 job at UMiami located?

This Clinical Research Coordinator 1 position at UMiami is located in Miami, FL (On-site). Always check UMiami's application page for specific state eligibility or relocation policies.

What qualifications are required for Clinical Research Coordinator 1 at UMiami?

For the Clinical Research Coordinator 1 role, UMiami highlights 1+ year of relevant experience; a bachelor's degree; experience with Clinical research protocol coordination, Chart review and pre-screening, Data collection and maintenance, Adverse event reporting, Regulatory compliance, Attention to detail. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.

How do I apply for the Clinical Research Coordinator 1 position at UMiami?

This listing links directly to UMiami's Workday application page. You can apply directly on UMiami's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.