University of Miami · 2 days ago
Clinical Research Coordinator 1 - CRANE Lab
The University of Miami is seeking a Clinical Research Coordinator 1 to work at the UHealth campus. This role involves managing simple clinical research protocols, coordinating study activities, and ensuring compliance with regulatory requirements.
Higher Education
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 the appropriate fundamental requirements of all international, national, and local regulatory bodies
Knows the contents and maintenance of study-specific clinical research regulatory binders
Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies
Adheres to University and unit-level policies and procedures and safeguards University assets
Assist with recruitment, screening, and enrollment of study participants in both community and hospital settings
Schedule and conduct study visits, assessments, and interviews either in-person or remotely
Collect, record, and enter data accurately into study databases and electronic case report forms (eCRFs)
Support participants in adhering to lifestyle and behavioral intervention protocols, including diet, exercise, and psychosocial components
Provide clear instructions and materials to participants and offer ongoing support throughout study participation
Maintain up-to-date and organized study documentation in accordance with regulatory and institutional requirements
Coordinate communications among research team members, clinical staff, community partners, and investigators
Assist in the development and distribution of culturally appropriate study materials for diverse participant populations
Report adverse events and protocol deviations promptly in collaboration with the study team
Participate in team meetings, study trainings, and quality assurance activities to ensure protocol compliance and participant safety
Qualification
Required
Bachelor's degree in relevant field required
Minimum 1 Year Of Relevant Experience Required
Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands
Ability to work collaboratively with others and contribute to a team environment
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
Medical
Dental
Tuition remission
And more
Company
University of Miami
At UM you'll join a diverse and energized academic community.
H1B Sponsorship
University of Miami has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (208)
2024 (151)
2023 (149)
2022 (121)
2021 (95)
2020 (114)
Funding
Current Stage
Late StageLeadership Team
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