Job Description

Department
 

BSD SUR - Transplant Surgery: Research - Islet Lab

About the Department
 

The Section of Transplantation is built on a strong history of surgical excellence, including the first-ever animal organ transplant in 1904. Over the years, the section has gone on to achieve many more 'firsts,' including the first successful living donor liver transplant and the first heart-liver-kidney transplant in the world. Today, UChicago Medicine is home to one of the busiest organ transplant centers in the nation and offers more transplant options than any other program in Illinois.

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
 

The job develops and implements programs to plan, direct, or coordinate the daily patient care activities in the Islet Lab under supervision of the Principal Investigator (PI), Dr. Piotr Witkowski. Ensures adherence to established clinical policies, protocols, regulations, and standards.

Responsibilities

• 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.).

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• Evaluates all lab results for signs of toxicity or complications related to either the treatment or disease.

• 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.

• Participates in established and future research programs.

• Provides assistance with IRB submissions.

• 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.

• 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.

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Work Experience:

Minimum requirements include knowledge and skills developed through 5-7 years of work experience in a related job discipline.

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Certifications:

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Preferred Qualifications

Experience:

• A minimum of 2 years of clinical patient experience.

Licenses and Certifications:

• 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.

Application Documents

• Resume (required)

• Cover Letter (required)

Job Family
 

Healthcare & Medical Services

Role Impact
 

Individual Contributor

FLSA Status
 

Non-Exempt

Pay Frequency
 

Biweekly

Scheduled Weekly Hours
 

40

Benefits Eligible
 

Yes

Drug Test Required
 

Yes

Health Screen Required
 

Yes

Motor Vehicle Record Inquiry Required
 

No

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.

 

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.

 

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