UNIV - Research Program Coordinator I - Journeyman - Department of Dermatology
About The Position
The Research Program Coordinator I provides support to Dermatology Research Programs. The coordinator adheres to study guidelines, coordinates study visits, confirms participants meet clinical inclusion criteria, and provides education to patients and families. The position also maintains study databases and documents, recruits research participants, and prepares for and conducts monitor and auditor visits. Some travel is required. The coordinator oversees day-to-day research protocol operations and project management, coordinates participant recruitment, screening, enrollment, and research visits, and supervises direct patient care activities related to research studies. The role supports investigators with consent procedures and regulatory compliance, manages and validates study data, prepares reports, coordinates sponsor monitoring visits, and serves as a liaison among internal teams and external research organizations, funding agencies, regulating bodies, and ancillary services.
Requirements
- Bachelor's degree.
- Two years of relevant program experience.
Responsibilities
- Serve as the primary administrative contact for internal research staff and operational liaison to other research organizations, funding agencies, and regulating bodies.
- Coordinate research visits with the research team and schedule visits according to protocol timelines.
- Manage data collection and entry, review documentation for accuracy and validity, and prepare study reports as needed.
- Oversee day-to-day operations of research protocols and provide project management for assigned projects.
- Supervise direct patient care activities for research participants.
- Coordinate and track recruitment, screening, and enrollment of research participants.
- Assist investigators with participant consent and adherence to regulatory procedures.
- Manage study data according to protocol requirements, maintain compliance, and submit study data on time.
- Implement corrective action plans as indicated.
- Coordinate monitoring visits with sponsors and prepare for sponsor visits in collaboration with the principal investigator.
- Review study workload and operating procedures to determine priorities and workflow.
- Liaise with ancillary services and provide protocol-related training as needed.
- Maintain study databases and complete study documents.
- Provide education to patients and their families.
- Recruit study patients and prepare for and conduct monitor and auditor visits.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
