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, Data management. Recruit and screen study participants. Obtain informed consent from participants”
What You'll Achieve.
Ensure data accuracy; Maintain patient safety; Meet study timelines
Industry & Context.
Troubleshooting; Data analysis
What They're Looking For.
Must Have
Bachelor's degree in a relevant field, Minimum of 2 years of clinical research experience, Experience with electronic data capture (EDC) systems, Knowledge of Good Clinical Practice (GCP) guidelines, Familiarity with Institutional Review Board (IRB) processes
Nice to Have
Master's degree in a related field, Experience with Epic EHR system, Certification in Clinical Research Professional (CCRC or CCRP), Experience in oncology research
What You'll Do.
Recruit and screen study participants
Obtain informed consent from participants
Collect and manage study data
Maintain study documentation and regulatory files
Monitor participant adherence to study protocols
Administer study-related procedures and assessments
Liaise with investigators and study sponsors
Ensure compliance with GCP and regulatory requirements
How You'll Work.
Team & Collaboration
Investigators; Study sponsors; Research staff
Communication Scope
Participant communication
Process & Methodology
Study 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 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. 6\. M
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