Registered Nurse - Clinical Research

Employer
US Oncology
Location
Eugene, Oregon
Salary
Competitive
Posted
Apr 22, 2021
Closes
May 20, 2021
Ref
4658
Contract Type
Permanent
Overview

WVCI_logo

WE WANT THE BEST TO JOIN OUR TEAM!

To get the best, we are offering a $2,500 sign-on bonus. 

 

Willamette Valley Cancer Institute and Research Center is actively seeking Registered Nurse to support our Clinical Research team. WVCI, which is part of The US Oncology Network, provides their patients with start of the art clinical trials to help patients on their journey through the cancer care continuum. This individual would be working directly with the patients taking part in the studies, coordinating with medical and research team involved. While clinical research experience is preferred, an individual with a passion for all things clinical and analytical will find success in this role. As the role has more administrative responsibilities than the average RN role, there is the possibility to work 1-2 days from home!

 

Employment Type: Full time, 1.0FTE/ 40 hr/week
Benefits: M/D/V, Life Ins., 401(k)
Location: Eugene, OR

JOB SCOPE:
Under direct supervision of a physician and nurse (if applicable), is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Collaborates with physician in determining eligibility of patients for clinical trials. Provides education to staff and patients. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.


Responsibilities

    Screens potential patients for protocol eligibility.Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol.Coordinates patient care in compliance with protocol requirements.May disburse investigational drug and provide patient teaching regarding administration.Maintains investigational drug accountability.In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.Responsible for accurate and timely data collection, documentation, entry, and reporting.Schedules and participates in monitoring and auditing activities.Maintains regulatory documents in accordance with USOR SOP and applicable regulations.Participates in required training and education programs.Responsible for education of clinic staff regarding clinical research.May collaborate with Research Site Leader in the study selection process.Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors.Provides a safe environment for patients, families, and clinical staff at all time through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

Qualifications

    Associate's degree in a clinical or scientific related discipline desired, Bachelor's degree preferred.RN License in OR REQUIREDMinimum two to three(2-3) year of experience in a clinical or scientific related discipline, preferably in oncology.Oncology research experience preferred.EMR experience preferred. SoCRA or ACRP certification preferred.
 CODES:

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