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Clinical Research Coordinator II

Quick overview

The CRCII manages all aspects of clinical trials, including subject screening, enrollment, and data collection from start-up to close-out. They partner with the Principal Investigator to expand amyloid research and ensure strict adherence to federal regulations and institutional policies.

Requirements summary

Requires a college degree and 2-5 years of related work experience. Preferred candidates have a bachelor's degree and 4 years of clinical research experience, specifically in amyloidosis, oncology, or heart failure.

bachelor degreeProject ManagementRegulatory ComplianceData EntrySpecimen ProcessingPatient RecruitmentPatient SchedulingInformed ConsentCommunity OutreachClinical Trial ManagementEPIC EMRCase Report FormsIRB Approvals

Job description

Department BSD MED - Cardiology - Clinical Research Staff About the Department The Section of Cardiology was founded in 1950 and has a proud history.
We are now charting a new course that will propel us to the forefront of cardiovascular medicine.
The strength of the Section reflects the quality and dedication of its faculty, trainees, and support staff and is enhanced by the rich environment at the University of Chicago.
The Section of Cardiology, within the Department of Medicine, is a highly collaborative workplace on the main campus of the University of Chicago.
Job Summary The Clinical Research Coordinator II (CRCII) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of a departmental or lab research manager.
While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRCII supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study.
By performing these duties with limited supervision and/or guidance, the CRCII works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.
Responsibilities Manages all aspects of conducting clinical trials including screening, consenting, enrollment, subject follow-up, completion of case report forms, adverse event reports, data entry, specimen collection, processing, and shipment.
Coordinates the conduct of the study from start-up through close-out, including recruitment, obtaining informed consent, screening study subjects, collecting research data, ensuring protocol adherence, and data integrity.
In partnership with the PI, expand amyloid clinical research to affiliated University of Chicago’s satellite sites and increase program reach through community education and outreach regarding amyloidosis.
Plans and coordinates patient schedules for study procedures, return visits, and study treatment schedules.
Performs assessments at visits and monitors for adverse events.
Organizes and attends site visits from sponsors and other relevant study meetings.
Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, drug dispensing logs, and study related communication.
Ensures compliance with federal regulations and institutional policies.

Benefits

Paid Time Off
Health Insurance
Retirement

4 years clinical research experience, minimum 2 years with amyloidosis, oncology, heart failure or experience in related disease process. Leadership and clinical project management.
Technical
Skills or
Knowledge: Human specimen processing and shipping. Working knowledge coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials). Preferred Competencies Excellent communication skills, orally and written. Create and deliver presentations. Develop and manage interpersonal relationships. Ability to multi-task successfully. Prioritize work appropriately and meet deadlines. Work autonomously, effectively, and collegially. Facilitate collaboration between university and hospital leadership. Familiarity with EPIC – electronic medical record. Working Conditions This is an on-site position. This role is patient-facing. Application Documents Resume/CV (required) Cover Letter (required) When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application. Job Family Research Role Impact Individual Contributor Scheduled Weekly Hours 40 Drug Test Required Yes Health Screen Required Yes Motor Vehicle Record Inquiry Required No Pay Rate Type Salary FLSA Status Exempt Pay Range $60,000.00 - $75,000.00 The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting. Benefits Eligible Yes The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook. Posting Statement The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination. Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form. All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position. The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information.
The
Report can be accessed online at: http://securityreport.uchicago.edu. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637. The University of Chicago is an urban research university that has driven new ways of thinking since 1890. Our commitment to free and open inquiry draws inspired scholars to our global campuses, where ideas are born that challenge and change the world. We empower individuals to challenge conventional thinking in pursuit of original ideas. Students in the College develop critical, analytic, and writing skills in our rigorous, interdisciplinary core curriculum. Through graduate programs, students test their ideas with UChicago scholars, and become the next generation of leaders in academia, industry, nonprofits, and government. To learn more about the university click here http://www.uchicago.edu/

Clinical Research Coordinator II

Quick overview

Requirements summary

Job description

Benefits

Minimum Qualifications

Preferred Qualifications

Experience

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