Clinical Research Coordinator 1
On-siteMiami, Florida, United States or Coral Gables, Florida, United States
Job Summary
Conduct chart review and pre-screening activities for study participant eligibility while maintaining enrollment procedures according to protocol. Coordinate routine clinical study activities including data collection, timeline planning, and appointment scheduling. Perform moderate to complex research tests and experiments, adapting procedures for quality improvement under supervision. Operate clinical research equipment following technical instructions and problem-solve operational failures. Assist in observing and reporting adverse events, advocating for study participants and quality standards throughout the study lifespan. Identify and report protocol deviations and unanticipated occurrences while adhering to international, national, and local regulatory requirements. Maintain study-specific regulatory binders and complete mandatory training in safety, equality, and research competencies. Work evenings, nights, and weekends as necessary.
Required Qualifications
- Bachelor's degree in relevant field
- Minimum 1 year of relevant experience
- Skill in completing assignments accurately and with attention to detail
- Ability to analyze, organize and prioritize work under pressure while meeting deadlines
- Ability to process and handle confidential information with discretion
- Ability to work evenings, nights, and weekends as necessary
- Commitment to the University's core values
- Ability to work independently and/or in a collaborative environment
- Mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies
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