University of Miami
Clinical Research Coordinator 2
Miami, FL · Staff+ · Contract
Sponsorship not specifiedDetected 12 hours ago
HRISClinical TrialsClinical ResearchHealth LiteracyPatient CareResearchCommunication
About the role
- To learn how to apply for a faculty or staff position, please review this tip sheet.
- The department of Medicine has an exciting opportunity for a full-time Clinical Research Coordinator 2 to work on the UHealth campus.
- 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.
Responsibilities
- Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols.
- Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
- Maintains study binders and filings according to protocol requirements, UM and department policy.
Requirements
- Bachelor's degree in relevant field required
- Minimum 2 years of relevant experience required
Skills
- Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
- Skilled in using office software, technology, and relevant computer applications.
- Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
Benefits
- Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.
- Adheres to cultural competency guidelines; implements strategies to meet study participants' needs for language translation, health literacy, etc.
- Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
Visa & Work Authorization
- mentation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines
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