Research Nurse 2 - Pediatric Oncology (Hybrid)

Pediatric Hematology/Oncology Research Nurse 2 - Hybrid

The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over 30 departments across Stanford University. We seek a Research Nurse 2 to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education and outreach. Given the SCI's mission, breadth, and depth, it employs over 320 staff members in a fast-paced, team-oriented, and forward-thinking environment with tremendous opportunities for personal and professional growth. The Clinical Trials Office (CTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting. You will be working with an unparalleled leading-edge community of faculty and staff who are fundamentally changing the world of health care in the cancer cellular therapy arena.

Reporting to the Pediatric Hematology/Oncology Clinical Research Nurse Manager, the Research Nurse 2 will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to safely enroll and maintain follow-up for children and adults in Pediatric Oncology studies. We are seeking candidates with excellent communication, organization, prioritization, multi-tasking and clinical skills. Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative and flexibility. Responsibilities include understanding and knowledge of currently open studies and acting as a resource for both faculty and clinical research staff.

DESIRED QUALIFICATIONS:

• Pediatric Oncology experience highly desired (Pediatric or neonatal nursing experience acceptable).
• Experience in clinical research.
• Experience with EMR system (EPIC).

PHYSICAL REQUIREMENTS*:

• Frequently stand/walk, sit, perform desk-based computer tasks, use a telephone, writing by hand, sort/file paperwork or parts, twist/bend/stoop/squat, and grasp lightly/fine manipulation.
• Occasionally reach/work above shoulders, grasp forcefully, operate foot and/or hand controls.
• Rarely kneel/crawl, climb (ladders, scaffolds, or other), scrub/sweep/mop/chop/mix, operate a manual pipette.
• • Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS:

• May be required to work with, take specific precautions against, and/or be immunized against potentially hazardous agents.
• May be exposed to blood borne pathogens.
• On call 24 hours/day.
• Frequent travel, might include international travel.

WORK STANDARDS:

• Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
• Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
• Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University''s Administrative Guide, http://adminguide.stanford.edu.

Core Duties:

• Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians.

• Provide clinical and administrative nursing support and oversight for research clinical trials based on scope of practice. Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies.

• Develop and manage budget for research study, and oversee resources including funds, personnel, and equipment as needed. Coordinate and collaborate with principal investigator to review study protocol and assess and analyze feasibility, budget projections, and staffing needs.

• Conduct study participant evaluations according to the study protocol, assess adverse events, and apply triage and judgment to determine course of action.

• Oversee and potentially administer medications and treatments per study protocol for out study participant research participants.

• Comply with institutional policies, standard operating procedures, and guidelines, and prepare and submit documentation as required by the study protocol, study sponsor, and regulatory authorities. Interpret complex protocols and regulatory requirements. Oversee and manage essential regulatory documents and handle confidential information (verbal and written) with tact and diplomacy, adhering to all HIPAA guidelines.

• Supervise non-clinical research staff as needed.

• Identify, recruit, and enroll study participants, as well as maintain study participant records and determine study participant criteria.

• Host external audits (Food and Drug Administration, National Institutes of Health, etc.).

• Support sponsor investigator research with Investigational New Drug/Investigational Device Exemption applications.

Minimum Education:

Bachelor's degree in nursing or equivalent

Minimum Experience:

Five years of experience in nursing, with at least two years in a research setting.

Knowledge, Skills and Abilities:

• Demonstrated ability to work with research subjects of all ages and backgrounds.

• Verbal and written communication skills to convey medical and research-related information to research subjects of all ages and backgrounds.

• Ability to identify confidential and sensitive information (written and verbal).

• Ability to implement good clinical practices in all interactions with study participants, their families, and colleagues.

• Ability to identify adverse reactions to study treatments and the required study protocol documentation to record these activities.

• Ability to implement study protocols with minimal supervision.

• Ability to provide work direction to research support staff.

• Demonstrate understanding of good clinical practices and regulatory compliance.

• Demonstrated experience with electronic data capture, including database management.

• Demonstrated ability to perform the functions of the position with minimal supervision.

Certificates and Licenses Required

Current license as a California Registered Nurse.

Certified Research Administrator or Clinical Research Coordinator preferred.

Current basic CPR certification.

Core Duties:

• Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians.

• Provide clinical and administrative nursing support and oversight for research clinical trials based on scope of practice. Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies.

• Develop and manage budget for research study, and oversee resources including funds, personnel, and equipment as needed. Coordinate and collaborate with principal investigator to review study protocol and assess and analyze feasibility, budget projections, and staffing needs.

• Conduct study participant evaluations according to the study protocol, assess adverse events, and apply triage and judgment to determine course of action.

• Oversee and potentially administer medications and treatments per study protocol for out study participant research participants.

• Comply with institutional policies, standard operating procedures, and guidelines, and prepare and submit documentation as required by the study protocol, study sponsor, and regulatory authorities. Interpret complex protocols and regulatory requirements. Oversee and manage essential regulatory documents and handle confidential information (verbal and written) with tact and diplomacy, adhering to all HIPAA guidelines.

• Supervise non-clinical research staff as needed.

• Identify, recruit, and enroll study participants, as well as maintain study participant records and determine study participant criteria.

• Host external audits (Food and Drug Administration, National Institutes of Health, etc.).

• Support sponsor investigator research with Investigational New Drug/Investigational Device Exemption applications.

Minimum Education:

Bachelor's degree in nursing or equivalent

Minimum Experience:

Five years of experience in nursing, with at least two years in a research setting.

Knowledge, Skills and Abilities:

• Demonstrated ability to work with research subjects of all ages and backgrounds.

• Verbal and written communication skills to convey medical and research-related information to research subjects of all ages and backgrounds.

• Ability to identify confidential and sensitive information (written and verbal).

• Ability to implement good clinical practices in all interactions with study participants, their families, and colleagues.

• Ability to identify adverse reactions to study treatments and the required study protocol documentation to record these activities.

• Ability to implement study protocols with minimal supervision.

• Ability to provide work direction to research support staff.

• Demonstrate understanding of good clinical practices and regulatory compliance.

• Demonstrated experience with electronic data capture, including database management.

• Demonstrated ability to perform the functions of the position with minimal supervision.

Certificates and Licenses Required

Current license as a California Registered Nurse.

Certified Research Administrator or Clinical Research Coordinator preferred.

Current basic CPR certification.