- To serve as primary coordinator for clinical research studies and supporting more senior team members.
- To provide a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance. May provide oversight to junior clinical research coordinators (CRC) and clinical research nurse coordinators (CRNC) in review of study documents.
- To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).
- To provide quality care to participants and their families within the area of clinical specialty.
- To coordinate the life cycle of the study from start-up through maintenance to closure.
- To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
- To perform the informed consent process following GCP.
- To act as a liaison between the clinical and research staff, departments, ancillary services, and the study sponsor to ensure protocol compliance throughout the study.
- Responsible for entering data into REDCap via iPad and reporting any protocol deviations.
- Uses FaceTime/Zoom calls, text messages, and phone calls to interact with the participant, based on the protocol.
- Ensures consistent interpretation and adherence to protocols at all stages of trials by team members.
- Recommends changes in protocols to improve the quality of data.
- Performs neurocognitive, vision, and physical fitness tests.
- Identifies and screens potential study participants to verify eligibility, and recruit/enroll participants. Once the individual is enrolled, is responsible for explaining and training participants on how to use the electronic REDCap survey application.
- Reviews electronic medical records to determine what, if any, treatments/services participants receive during the study period, and how those treatments may affect study outcomes.
- Attends research study meetings to discuss the progress/status of the study participants.
- Supports other research staff as needed on participant assessments and follow-ups. Collaborates with and maintains a positive rapport with school and university research staff, study sites, and members of the research team, as well as federal granting agencies.
- Assists with revision of REDCap based on the protocols.
- Performs other duties as assigned.
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Clinical Research Nurse Coordinator II - University, United States - University of Alabama at Birmingham
Description
The University of Alabama at Birmingham (UAB), Department of Nursing Family, Comm & Health Systems, is seeking a Clinical Research Nurse Coordinator II.
The CRNC II works directly with study participants to deliver a telehealth-based physical activity protocol.Responsibilities include exergame equipment setup (travel to participant's home or working with on-site staff), exergame system safety instruction, personalized exergame prescription development/adjustment, exergame coaching, discussion of barriers strategies, review of exergame minutes, QA about the exergame prescription.
General ResponsibilitiesAnnual Salary Range:
$60,835 - $98,855
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement. Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.
