at University of Illinois at Chicago in Chicago, Illinois, United States
Job Description
Clinical Research Coordinator - Neurosurgery
Clinical Research Coordinator - Neurosurgery
Hiring Department: Neurosurgery
Location: Chicago, IL USA
Requisition ID: 1025473
Posting Close Date: 08/21/2024
About the University of Illinois Chicago
UIC is among the nation's preeminent urban public research universities, a Carnegie RU/VH research institution, and the largest university in Chicago. UIC serves over 34,000 students, comprising one of the most diverse student bodies in the nation and is designated as a Minority Serving Institution (MSI), an Asian American and Native American Pacific Islander Serving Institution (AANAPSI) and a Hispanic Serving Institution (HSI). Through its 16 colleges, UIC produces nationally and internationally recognized multidisciplinary academic programs in concert with civic, corporate and community partners worldwide, including a full complement of health sciences colleges. By emphasizing cutting-edge and transformational research along with a commitment to the success of all students, UIC embodies the dynamic, vibrant and engaged urban university. Recent "Best Colleges" rankings published by U.S. News & World Report, found UIC climbed up in its rankings among top public schools in the nation and among all national universities. UIC has over 300,000 alumni, and is one of the largest employers in the city of Chicago.
Description:
Position Summary
Department of Neurosurgery at the University of Illinois Chicago is seeking a Clinical Research Coordinator.
The Clinical Research Coordinator manages and directs the coordination and timely handling of all components of clinical research protocols in Neurosurgery; including pre and post research activities, in and outside of the clinical setting. This position is responsible for the implementation and conduct of multiple research projects. Develops effective patient recruitment strategies. Coordinates comprehensive patient protocol treatment schedules to maintain compliance to protocol requirements. Oversee and participate in subject recruitment, screening, scheduling, testing, and data management for a multi-faceted investigation.
Duties & Responsibilities
Assist in the establishment, and coordinates the implementation, of clinical protocol priorities and organization structure.
Notify and inform physicians, clinical staff, and affiliates and grant sponsors of adverse events and protocol modifications, including their impact on the clinical research.
Coordinate the activation and maintenance of clinical protocols, including review and completion of submissions, amendments, and adverse event reports as required by the UIC Institutional Review Board (IRB), Protocol Review committee and grand sponsors.
Review laboratory and clinic procedures and evaluations regularly that they meet protocol compliance.
Act as a liaison between physicians, clinical staff and the UIC IRB office, grant sponsors and regulatory agencies to ensure priorities are clearly communicated and resources are allocated appropriately across multiple ongoing projects.
Assist physicians and clinical staff in identification, recruitment and enrollment strategies of patients to increase enrollment and to meet clinical research protocols
Coordinate outreach to and liaison with staff at schools, community clinics, science fairs, etc. to make research presentations and recruit new clients for various research projects.
Execute informed consent process and monitor patient status; enroll clients in programs, explaining the research protocols to the clients and parents and obtain appropriate consent forms.
Ensure that client enrollment and research activities comply with established protocols, regulatory and monitoring agency standards and grans sponsor guidelines.
Participate in conducting surveys of clients and parents.
Collect and review client evaluations/assessments, surveys, and participation interviews to develop reports for the PI and appropriate agencies and grant sponsors.
Assist investigators in organizing study data for grant reports, analysis for meeting presentations and publications.
Perform other related duties and participate in special projects as assigned.
Qualifications:
Minimum Qualifications
Bachelor degree in nursing, science, or a health related field required.
Certified Clinical Research Coordinator (CCRC)... For full info follow application link.
The University of Illinois may conduct background checks on all job candidates upon acceptance of a contingent offer. Background checks will be performed in compliance with the Fair Credit Reporting Act.
The University of Illinois Chicago is an affirmative action, equal opportunity
institution/employer and does not discriminate on the basis of race, color, national origin, sex, religion, age, sexual orientation, gender identity, veteran or disability status, height, weight, or marital status in employment or the provision of services.
