at University of Illinois at Chicago in Chicago, Illinois, United States
Job Description
Senior Clinical Research Coordinator II (Research Studies Manager)
Senior Clinical Research Coordinator II (Research Studies Manager)
Hiring Department: Office of Population Health Sciences
Location: Chicago, IL USA
Requisition ID: 1026402
Posting Close Date: July 23, 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 - SR Clinical Research Coordinator II (Research Studies Manager).
General Job Summary:
The Office of Population Health Sciences (OPHS) at UIC is seeking applications for a Senior Clinical Research Coordinator II (Research Studies Manager). This Position is responsible for managing and overseeing the day-to-day operations of clinical research studies, recruiting, scheduling and screening study participants, as well as documenting and reporting on the daily operations of assigned research studies/clinical trials. Working in collaboration with the Principal Investigator, the SR CRC II/Research Studies Manager is responsible for the oversight, facilitation and coordination of the daily research activities and plays a critical role in the conduct of the study. The SR CRC II/Research Studies Manager works collaboratively with the entire clinical research team, sponsors, and associates to ensure productivity, quality, and timely completion of studies. The SR CRC II/Research Studies Manager is expected to support, guide, train, demonstrate and lead clinical research team members in the implementation of clinical research related activities. This position applies critical thinking and creative problem-solving skills across a wide variety of clinical research studies, and contributes to the development of new processes, procedures, tools and training to enhance clinical research activities and is accountable for adhering to quality standards. They perform a variety of data management duties of a complex and technical nature in support of clinical research studies to ensure adherence to protocols and quality of information received.
Duties & Responsibilities
RESEARCH, DATA & PROTOCOL MANAGEMENT
Lead within the department to improve clinical research practices and operations across studies and serve as a resource to others.
Oversee and participate in coordinating and conducting complex clinical research studies, ensuring compliance with federal and institutional regulations.
Take initiative in establishing and coordinating the implementation of clinical research protocol priorities and organizational structure based on study needs, identifying areas for improvement.
Execute project goals and tasks as outlined in the project plan by actively assuming responsibility for components necessary for timely completion.
Lead protocol changes, assessing and coordinating with various departments to implement changes.
Maintain working knowledge of current protocols and internal Standard Operating Procedures (SOPs) and disseminate information on any changes to all stakeholders.
Collaborate with the Principal Investigator (PI), department, sponsor, and institution to support and guide the administration of compliance, financial, personnel, and other related aspects of clinical studies.
Prepare, submit, and assist Investigators with multiple levels of research... 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.
