Clinical Research Nurse Practitioner, Seattle Vaccine Trials Unit

Job ID
17607
Type
Regular Full-Time
Company
Fred Hutchinson Cancer Research Center
Location
US-WA-Seattle
Category
Advanced Practice Providers

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here. 
 
The Seattle Vaccine Trials Unit (VTU) (click here to visit their webpage) is a program within the Vaccine & Infectious Disease Division of Fred Hutchinson Cancer Research Center. Led by Principal Investigator Julie McElrath, the VTU is funded to conduct phase I, II, and III clinical trials. As a clinical research site, the VTU is responsible for the recruitment, selection, and enrollment of study participants, and immunization and clinical monitoring of these participants in clinical trials of investigational agents being studied for the prevention of HIV, SARS-CoV-2, and other infectious diseases. 
  
The Clinical Research Nurse Practitioner, coordinates, and implements clinical research studies involving human subjects for the Immunology & Vaccine Development research program. The primary focus of the Clinical Research Nurse is screening, enrolling, and following study participants. The position will require willingness to work with COVID-19 and HIV prevention modalities (vaccines, immunoprophylaxis, etc.) as well as working in settings where individuals with active COVID-19 infection will be seen. This position will likely work at the unit’s remote and mobile sites, so flexibility in travel and hours will be important. 

Responsibilities

The incumbent works under the supervision of the Principal Investigator as part of a clinical research team including the VTU physicians, other clinicians, and other unit personnel. Direct supervision will be by the remote/mobile unit’s supervising clinician. The position requires the performance of responsibilities with a high level of independence within the scope of study protocol(s) and guidelines. 

  • Determine participant study eligibility, obtain informed consent, and initiate participant randomization and enrollment in research studies in accordance with regulatory and GCP guidelines and institutional policy including:
    • Provide a complete explanation of a study to potential volunteers so as to obtain informed consent
    • Conduct phone (or other remote) visits for protocols involving off-site screening, enrollment, and electronic consenting
    • Record and evaluate medical histories as well social and sexual histories (if required by protocol)
    • Draw blood for screening labs if required per protocol, and interpret the results for inclusion/exclusion criteria, as well as for medical follow-up if needed
    • Provide pregnancy prevention counseling for women, including contraceptive counseling as needed
    • Perform complete physical exams and complete other physical exam assessments per protocol requirements
  • Follow study protocol for each participant visit
  • Perform clinical procedures including vital signs, vaccine administration, blood draws, IV infusions, and physical exam assessments
  • Able to perform, or willing to learn skills to perform, mucosal biopsy procedures including collection of vaginal, cervical, and rectal biopsy samples
  • Maintain appropriate source documentation and complete case report forms/electronic case report forms
  • Identify, assess, and report adverse events in accordance with protocol and regulatory guidelines and institutional policy
  • Provide various forms of health education to study participants and provide appropriate referrals to community medical, social, substance abuse and mental health programs if needed.
  • Help to maintain the compliance of participants with protocol visit schedule
  • Provide support for community education and recruitment with the VTU community educator, recruitment coordinator, and recruiters
  • Assist the clinic coordinator and/or the supervising clinician in managing the daily operations of a research study
  • Assist the clinic coordinator and/or the supervising clinician in developing tools for study implementation including data collection tools and study reference materials
  • Provide leadership and guidance to program/research/clinical assistants in the execution of their duties relative to protocol implementation and conduct
  • Maintain thorough knowledge in the field through attending related project meetings and symposia, reading related literature, and maintaining professional associations 

Qualifications

  • Current WA state ARNP license with a minimum of one year of post-certification clinical experience required. 
  • This position will support our remote and mobile clinics so travel within WA State and flexible hours will be necessary. Will require weekend and evening hours. 
  • Two years of clinical research experience is strongly preferred.   
  • Previous experience in clinical data collection is preferred.   
  • Strong written and verbal communication skills including computer skills, proficiency with MS Word, Excel and PowerPoint are essential.  
  • The ideal candidate should be culturally fluent, comfortable and aware of various community backgrounds and perspectives. Experience working with underrepresented and marginalized communities, including communities of color, transgender individuals, and the LGBTQ+ community is preferred. 
  • Knowledge of Spanish is helpful.

Our Commitment to Diversity

We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to our Employee Services Center at hrops@fredhutch.org or by calling 206-667-4700.

Options

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed