Clinical Research Coordinator I, Family and Community Medicine

Position Highlights

This position participates in the design, development, execution, and initial interpretation of clinical trials and/or related service projects. Prepares, coordinates, and maintains all regulatory documentation, including IRB submissions, approvals of new or revised protocols, safety reports, and progress reports. Participates in data management design and maintenance; assists in data analysis. Provides team coordination, communication, training, and quality control. Develops standard operating procedures, compliance forms, and tracking documents.

• Visa sponsorship is not available for this position.

Duties & Responsibilities

• Recruits, screens, and enrolls agencies and participants who meet project criteria.
• Collects basic information through surveys and contacts.
• Maintains telephone, video conference, and in-person contact.
• Notifies project director and supervisor of participant status.
• Assists in the development, coordination, and deployment of project protocols with agencies and participants.
• Performs trainings and consultations with agencies and participants according to project protocols.
• Collects participant data, enters and analyzes data, and compiles reports, adhering to project protocols.
• Keeps appropriate logs, tracks participants, and prepares project materials.
• Prepares documentation, reports, graphs, and other materials.
• Coordinates and manages project communications and meetings with outside entities.
• Coordinates, facilitates, and manages project agendas, communications and meetings with project personnel.
• Submits project protocols and amendments, consent forms, and recruiting materials to the University of Arizona Institutional Review Board and department for approval with oversight from supervisor.
• Coordinates and maintains all regulatory reviews with project funders, stakeholders and the University of Arizona.