University of Miami

Healthcare

ClinicalResearchCoordinator2

$1–1k Miami, Florida, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Clinical Research Coordinator 2 at University of Miami. Skills: Clinical research, Patient care, Regulatory compliance. Coordinate clinical research studies. Recruit and screen study participants”

What You'll Achieve.

Ensure study integrity; Meet enrollment targets; Maintain data accuracy

Industry & Context.

Healthcare
Problems you'll solve

Problem resolution

What They're Looking For.

Must Have

Bachelor's degree, 2 years of experience in clinical research, Experience with data collection, Experience with patient recruitment, Experience with regulatory compliance

Nice to Have

Master's degree, Experience with Epic EHR, Experience with clinical trial management software

What You'll Do.

Coordinate clinical research studies

Recruit and screen study participants

Collect and manage study data

Ensure compliance with regulatory requirements

Maintain study documentation

Assist with study protocol development

Communicate with study sponsors and investigators

Monitor participant safety and well-being

How You'll Work.

Team & Collaboration

Research team; Physicians; Nurses; Study sponsors

Communication Scope

Participant communication; Investigator communication

Process & Methodology

Project coordination

Full Job Description

**_Current Employees:_** If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click [here](https://www.myworkday.com/umiami/d/task/1422$7248.htmld) 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](https://my.it.miami.edu/wda/erpsec/tipsheets/ER_eRecruiting_ApplyforaJob.pdf). The University of Miami/UHealth Department of SCCC- CRS has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work at the UHealth campus in Miami, Fl. **CORE JOB SUMMARY** The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel. **CORE JOB FUNCTIONS** 1\. Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility. 2\. Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols. 3\. Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations. 4\. Maintains study binders and filings according to protocol requirements, UM and department policy. 5\. Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.

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