Job Information
UNIVERSITY OF TEXAS AT AUSTIN Clinical Research Coordinator in Austin, Texas
Participate in planning, implementation and execution of the conduct of sponsored clinical trials and grant funded research. Coordinate and review research study procedures to ensure receipt, completeness and accuracy of study data. Coordinate assigned projects with an emphasis on communication with research sponsors, community partners, clinical services, and university administrators, investigators and research team members. Experience coordinating clinical research in acute hospital settings and extracting data from medical records.Screen, recruit, and enroll potential research subjects and track participation over time. Conduct and manage study visits. Deliver participant training materials and programs. Conduct participant interviews and measurements.Complete informed consent processes and data collection procedures. Facilitate institutional review board (IRB) applications, submissions, and updates. Assist in preparation of annual reports for federal, state, and local agencies. Inform IRB of amendments to research studies.Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols. Monitors and reports on progress of projects. Assists with finding and applying for research funding.Monitor adherence to procedures/protocols to ensure optimal subject participation rates and accurate data collection and reporting. Ensure completion of contract requirements and project specifications. Facilitate project collaborations as assigned.Enters data into study specific databases. Ensures data remains clean and coded appropriately. Maintains impeccable study records. Maintains log tracking progress of all trauma related research studies and reports on progress to appropriate departments/groups. Serves as a liaison between clinical setting and research investigators to ensure clear communication and study progress. Other related functions as assigned including developing standard operating procedures for clinical research activities.Other related duties as assigned.