at University of Illinois at Chicago in Chicago, Illinois, United States
Job Description
Visiting Clinical Research Coordinator - Department of Medicine, Division of Pulmonary
Visiting Clinical Research Coordinator - Department of Medicine, Division of Pulmonary
Hiring Department: Pulmonary, Critical Care, Sleep and Allergy
Location: Chicago, IL
Requisition ID:1026310
Posting Close Date: August 2, 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:
Protocol Management
Assist in establishing and coordinating the implementation of clinical research protocol priorities and organization structure.
Conduct research visits as specified by the protocol.
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 grant sponsors.
Coordinate and track IRB submissions and maintenance.
Review laboratory and clinical procedures and evaluations regularly to ensure protocol compliance.
Assists in completing a Materials Transfer Agreement as needed
Client Enrollment and Protocol Compliance
Complete recruitment of 120 participants (2 per week).
Coordinate and attend meetings with graduate student (Research Assistant), co-investigators, and collaborators.
Ensure that participant enrollment and research activities comply with established protocols, regulatory and monitoring agency standards, and grant sponsor guidelines.
Participate in conducting surveys of participants and supporting family/friends.
Coordinate and provide data management using REDCAP.
Remain competent and current through self-directed learning, developing contacts with research equipment support services, online data management and UIC CCTS, and attending training and/or seminars.
Assure the timely completion of participant recruitment by performing all other duties as assigned.
Perform other related duties and participate in special projects as assigned.
Qualifications:
Bachelor degree required; at least one year experience in a research discipline required. Experience in a clinical research setting, experience working with Federal Regulations and IRB's required.
Ability to manage multiple tasks. Strong interpersonal and customer service skills. Requires excellent communication, organization, presentation and computer/pc skills. Proficiency in Microsoft Office and basic statistical analysis (using R, STATA, or other software) is preferred.
Prior experience with REDCap (online biomedical research data management tool), working with patients in research settings
Knowledge of research protocols, principles and procedures; knowledge of aspects of clinical trials such as screening, interviewing, case reports forms; knowledge of experimental design, mathematics, statistics, computer applications and computer data management; oral and written communication skills; knowledge of a science such as biology or psychology; ability to identify, produce, organize, evaluate and interpret data; knowledge of ethics and regulatory procedures (i.e. informed consent, IRB applications, data safety and monitoring plans) involved with clinical trials and other clinical research; ability to work as a member of a... 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.
