University of Miami
Healthcare
ClinicalResearchCoordinator1
Neural analysis suggests this role is
optimal for Entry candidates.
“Clinical Research Coordinator 1 at University of Miami. Skills: Clinical research protocols, Data collection, Participant advocacy. Perform chart review/pre-screening. Maintain enrollment procedures”
Industry & Context.
Problem solve operational failures; Problem solve protocol deviations; Problem solve unanticipated occurrences
Local travel may be required
What They're Looking For.
Must Have
Bachelor's degree in relevant field, Minimum 1 year of relevant experience
Nice to Have
Bilingual in English and Spanish
What You'll Do.
Perform chart review/pre-screening
Maintain enrollment procedures
Coordinate clinical study activities
Collect and maintain data
Schedule appointments and visits
Perform research tests/experiments
Adapt procedures for quality improvement
Follow technical instructions
Problem solve operational failures
Observe adverse events
Inform PI/supervisor of adverse events
Address adverse events per protocol
Advocate for study participants
Maintain quality standards
Identify protocol deviations
Report protocol deviations
Problem solve protocol deviations
Identify unanticipated occurrences
Report unanticipated occurrences
Problem solve unanticipated occurrences
Follow regulatory body requirements
Maintain study binders
Maintain training in safety
Maintain training in equality
Maintain training in responsible conduct
Maintain continuing education
Maintain research competencies
Adhere to University policies
Adhere to unit-level policies
Safeguard University assets
Assist with participant recruitment
Assist with participant retention
Screen potential study participants
Distribute study drug materials
Assist in implementing protocol amendments
Assist with study orientation
Assist with in-services for research team
Assist with in-services for clinical staff
Monitor protocol implementation
Monitor study progress
Keep investigators apprised of study
Submit progress reports
Assist with communications
Interact with sponsors
Interact with data coordinating centers
Interact with compliance monitors
Interact with collaborators
Interact with investigators' personnel
Interact with academic personnel
Interact with administrative personnel
Interact with departments
Assist with administrative tasks
Document core competencies
Document certification mandates
Document safety education
Document responsible conduct education
Document performance reviews
Adhere to cultural competency guidelines
Implement strategies for participant needs
Meet participant needs for translation
Meet participant needs for health literacy
How You'll Work.
Team & Collaboration
Collaborative environment; Research team; Clinical staff
Process & Methodology
Plan study timelines
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 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. **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
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