Department
BSD SUR - Transplant Surgery: Research - Islet Lab
About the Department
What our surgeons can achieve in the operating room would not be possible without the ongoing work that is done in our laboratories, and this is especially true in the Section of Transplantation. Our researchers are well known for their basic science research in transplantation tolerance and clinical trial work around islet cell transplantation for diabetes.
Job Summary
Responsibilities
Clinical:
Leads patient post-transplant medical care in relation to study protocols under supervision of the PI.
Educates potential research subjects concerning clinical aspects of their disease, purpose and nature of the protocol, and impact on the patient should they agree to participate (i.e., treatment schema, tests, clinic visits, etc.).
Meets with patients in clinic and completes study visits and assessments as deemed necessary.
Evaluates all lab results for signs of toxicity or complications related to either the treatment or disease.
Coordinates all follow-up lab tests specified by the study and additional tests at the discretion of the PI to evaluate toxicities and treatment.
Teaches patients and their family members how to administer injections and signs and symptoms of side effects.
Covers on-call service to answer patient questions, which occur after business hours (e.g., nights, weekends, and holidays).
Works with PI to coordinate hospital admissions, transplant procedures, and study related tests.
Develops resources and materials for patient and family teaching, if none exist.
Provides family education depending on patient's illness and route of medication delivery.
Provides in-servicing and educating both the nursing units and lab staff regarding upcoming and ongoing protocols.
Research:
Participates in established and future research programs.
Provides assistance with IRB submissions.
Instructs the investigator and research staff on the submission process and provides instructional material for reference.
Works with PI, sponsoring agencies, Medicine Administration, and Office of Research Services to assist with amendment submission, changes or corrections to protocols/and or consent forms.
Works with administrators to submit and revise clinical trial agreements.
Assists in setting up regulatory documents, shadow file systems, databases, screening logs, adverse experience reporting mechanism, and regulatory binders.
Trains and participates in trial related activity from the initial entry to complete follow-up of patients enrolled into research protocols.
Reports adverse drug reactions and submits the appropriate documentation to the FDA, NCI and IRB.
Assists in recruiting patients for identified clinical trials.
Supervises and trains staff on proper data management techniques.
Provides cross coverage for other team members
Other:
Develops and implements treatment plans and provides guidance on therapies. Provides follow-up with patients.
Implements evaluation programs regarding the quality and effectiveness of nursing practice or organizational systems.
Guides clinical practices for patient care or research projects, such as by reviewing patient records, monitoring compliance, and meeting with regulatory authority.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Certifications:
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Preferred Qualifications
Education:
Master of Science in Nursing.
Experience:
Clinical patient experience.
Licenses and Certifications:
Current Advanced Practice Nurse (APN) license in the State of Illinois or eligibility to receive by start date.
Current Registered Nurse (RN) license in the State of Illinois or eligibility to receive by start date.
Preferred Competencies
Ability to provide direct patient care professionally and respectfully.
Excellent interpersonal skills.
Excellent verbal and written communication.
Extensive knowledge of Microsoft Word, Excel, PowerPoint, and Adobe Acrobat.
Working Conditions
Ability to work onsite 5 days per week.
Ability to take call on selected nights and weekends.
Ability to travel and participate in scientific conferences.
Ability to participate in research promotion events after normal working hours.
Application Documents
Resume (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
Role Impact
Scheduled Weekly Hours
Drug Test Required
Health Screen Required
Motor Vehicle Record Inquiry Required
Pay Rate Type
FLSA Status
Pay Range
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
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.
In addition to the base pay posted above, this position may be eligible for N/A
Posting Statement
The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, national or ethnic origin, 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.
Staff 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.
We seek a diverse pool of applicants who wish to join an academic community that places the highest value on rigorous inquiry and encourages a diversity of perspectives, experiences, groups of individuals, and ideas to inform and stimulate intellectual challenge, engagement, and exchange.
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