University of Miami
Healthcare
ClinicalResearchCoordinator2
Neural analysis suggests this role is
optimal for Mid candidates.
“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.
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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