The department of Psychiatry has an exciting opportunity for a full-time Clinical Research Coordinator 1 to work onsite on the UHealth campus.
Requirements
- Perform chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
- Coordinate routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
- Perform moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.
- Assist in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
- Identify, reports, and helps problem solve protocol deviations and unanticipated occurrences.
- Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
- Know the contents and maintenance of study-specific clinical research regulatory binders.
- Maintain requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
- Adhere to University and unit-level policies and procedures and safeguards University assets.
Benefits
- Competitive salaries
- Comprehensive benefits package including medical, dental, tuition remission and more
