Clinical Research Nurse Specialist

Updated: 3 months ago
Location: Chicago, ILLINOIS

Details

Posted: 05-Dec-23

Location: Chicago, Illinois

Type: Full-time

Salary: Open

Categories:


Other Staff/Administrative
Staff/Administrative

Internal Number: JR24678


Location: Chicago, IL

Job Description:

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.

Preferred Qualifications

Education:

  • Master of Science in Nursing.

Experience:

  • A minimum of 2 years of 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)

The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, status as an individual with a disability, protected 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 the Applicant Inquiry Form.

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: 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.


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