Clinical Research Coordinator- Surgery

Salary:
The budgeted salary range for the position is $54,000.00- $60,000.00.

The pay offered to the selected candidate will be determined based on factors including (but not limited to) the experience and qualifications of the selected candidate including equivalent years in rank, training, and field or discipline; internal equity; and external market pay for comparable jobs.

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.

This position is intended to be eligible for benefits . This includes Health, Dental, Vision, Life Insurance, a Retirement Plan, Paid time Off, and Tuition waivers for employees and dependents.

The Department of Surgery at the University of Illinois Chicago is seeking a Clinical Research Coordinator.

The Clinical Research Coordinator manages and coordinates the timely handling of all components of clinical research protocols, including pre and post research activities, that are internal and external to the clinical setting. This position is responsible for implementing and conducting multiple research studies for the surgery department. This includes coordinating patient consenting processes for both inpatient and outpatient settings, as well as managing the collection and handling of lab samples in accordance with protocol requirements.

Additionally, it involves coordinating detailed patient treatment schedules to maintain compliance to protocol requirements.

• Assist in establishing and coordinating the implementation of clinical research protocol priorities and organization structure for several research studies related to surgery.
• 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.
• Analyze retention rates and formulate plans to retain participants.
• Monitors patient status; explain the research protocols to the clients and supporting family/friends.
• 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.
• Consent patients…