Job Description

Visiting Clinical Research Coordinator – Division of Rheumatology

Hiring Department: Department of Medicine

Location:  Chicago, IL USA

Requisition ID: 1022440

Posting Close Date: December 19, 2023

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 nearly 260,000 alumni, and is one of the largest employers in the city of Chicago.

Description:

Position Summary
This position manages and directs the coordination and timely handling of all components of clinical research protocols, including pre- and post-research activities, both in and outside of the clinical setting. Responsible for the implementation and conduct of multiple research projects of all clinical phases, including budgeting and compliance. Additional responsibilities include activation and maintenance of various clinical protocols including review and completion of submissions, amendments, and adverse event reports as required by the UIC Institutional Review Board, Protocol Review Committee and sponsors; act as a liaison between physicians, clinical staff and UIC IRB office, sponsors, and regulatory agencies. Assist physicians and clinical staff in identification, recruitment, and enrollment of patients for clinical research protocols, including interacting with patients thus ensuring protocol compliance. Develops effective patient recruitment strategies.

Duties & Responsibilities

• Assist in establishing and coordinating the implementation of clinical research protocol priorities and organization structure.
• Notify and inform physicians, clinical/research staff, affiliates and grant sponsors of adverse events and protocol modifications, including their impact on the clinical research program.
• Responsible for management of all data related to the study
• 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.
• Review laboratory and clinical procedures and evaluations regularly to ensure protocol compliance.
• Act as 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.
• Communicate clinical information and work with stakeholders to create best practice tools.
• Client Enrollment and Protocol Compliance
• Assist physicians and clinical staff in identification, recruitment and enrollment strategies of patients to increase enrollment and to meet clinical research protocols.
• Analyze retention rates and formulates plans to retain participants.
• Coordinate outreach to and liaison with staff at schools, community clinics, science fairs, etc. to make research presentations and recruit new participants for various research projects.
• Execute informed consent process and monitors patient status; Enroll participants into programs, explaining the research protocols to the clients and supporting family/friends, and obtain appropriate consent forms.
• 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.
• Collect and review client evaluations/assessments, surveys, and participant interviews to develop reports for the PI and appropriate agencies and grant sponsors. Evaluate data to determine project effectiveness.
• Assist investigators in preparing study data, literature reviews, analysis for meeting presentations and publications.
• Perform other related duties and participate in special projects as assigned.

Qualifications:

Minimum Qualifications
Bachelor degree in nursing, mental health, psychology, pharmaceutical sciences, social science, or a related field required.
At least one year experience in a research discipline required.

Preferred Qualifications
Certified Clinical Research Coordinator (CCRC) preferred.

The University of Illinois System is an equal opportunity employer, including but not limited to disability and/or veteran status, and complies with all applicable state and federal employment mandates. Please visit Required Employment Notices and Posters to view our non-discrimination statement and find additional information about required background checks, sexual harassment/misconduct disclosures, COVID-19 vaccination requirement, and employment eligibility review through E-Verify.

The university provides accommodations to applicants and employees. Request an Accommodation

How to Apply

Job Categories: LGBT. Job Types: Full-Time. Salaries: 40,000 - 60,000.

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