4d ago
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Clinical Research Coordinator 1

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HealthcareClinical Researcher
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Quick Summary

Key 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.

Technical Tools
HealthcareClinical Researcher

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The Clinical Translational Research Site is currently seeking a full-time Clinical Research Coordinator 1 to work in Miami.

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.

Responsibilities

~1 min read
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    Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.

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    Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation. 

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    Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.

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    Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.

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    Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.

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    Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.

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    Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.

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    Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.

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    Knows the contents and maintenance of study-specific clinical research regulatory binders.

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    Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.

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    Adheres to University and unit-level policies and procedures and safeguards University assets.

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.

Full time

Requirements

~1 min read

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.

Staff

Location & Eligibility

Where is the job
Not specified
Location terms not specified
Who can apply
Same as job location

About this job

Posted
4 days ago
Employer
has 1,261 open jobs on Jobera.

Listing Details

Posted
October 12, 2026
First seen
October 14, 2026
Last seen
October 16, 2026

Posting Health

Days active
1
Repost count
0
Trust Level
49%
Scored at
October 16, 2026

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Clinical Research Coordinator 1