Biological Sciences Division at the University of Chicago
Clinical Research Nurse Specialist, Islet Lab
Biological Sciences Division at the University of Chicago, Chicago, Illinois, United States, 60290
Clinical Research Nurse Specialist, Islet Lab
Join the Biological Sciences Division at the University of Chicago as a Clinical Research Nurse Specialist within the Islet Lab.
Job Summary The Clinical Research Nurse Specialist manages post‑transplant patients and contributes to multiple studies within the Section of Transplant Surgery under the supervision of the Principal Investigator (PI). The incumbent will participate in a variety of clinical research projects/studies involving various modalities of treatment for patients, including multi‑centered cooperative group and intergroup trials at a national level, multi‑institutional pharmaceutical trials, and single and multi‑centered trials.
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.
Education
Minimum: College or university degree in a related field.
Preferred: Master of Science in Nursing.
Work Experience
Minimum: 5‑7 years of experience in a related job discipline.
Licenses and Certifications
Current Advanced Practice Nurse (APN) license in Illinois or eligibility to receive by start date.
Current Registered Nurse (RN) license in 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)
Compensation Base pay: $85,000 – $120,000 per year.
Benefits Eligible for the University of Chicago benefit programs, including health, retirement, and paid time off.
EEO Statement University of Chicago is an equal‑opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, disability, or other protected classes. For additional information please see the University’s Notice of Non‑Discrimination. For accommodation requests, contact 773‑702‑5800 or submit a request via the Applicant Inquiry Form.
Posting Statement All offers of employment are contingent upon a background check. The University considers conviction information on a case‑by‑case basis.
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Job Summary The Clinical Research Nurse Specialist manages post‑transplant patients and contributes to multiple studies within the Section of Transplant Surgery under the supervision of the Principal Investigator (PI). The incumbent will participate in a variety of clinical research projects/studies involving various modalities of treatment for patients, including multi‑centered cooperative group and intergroup trials at a national level, multi‑institutional pharmaceutical trials, and single and multi‑centered trials.
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.
Education
Minimum: College or university degree in a related field.
Preferred: Master of Science in Nursing.
Work Experience
Minimum: 5‑7 years of experience in a related job discipline.
Licenses and Certifications
Current Advanced Practice Nurse (APN) license in Illinois or eligibility to receive by start date.
Current Registered Nurse (RN) license in 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)
Compensation Base pay: $85,000 – $120,000 per year.
Benefits Eligible for the University of Chicago benefit programs, including health, retirement, and paid time off.
EEO Statement University of Chicago is an equal‑opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, disability, or other protected classes. For additional information please see the University’s Notice of Non‑Discrimination. For accommodation requests, contact 773‑702‑5800 or submit a request via the Applicant Inquiry Form.
Posting Statement All offers of employment are contingent upon a background check. The University considers conviction information on a case‑by‑case basis.
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