RN - Clinical Research Coordinator

The US Oncology Network•Eugene, OR

1d•Onsite

About The Position

The Willamette Valley Cancer Institute and Research Center is actively seeking an RN - Clinical Research Coordinator for our location in Eugene, Oregon. 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. This role will also support and adhere to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards.

Requirements

RN License in OR REQUIRED
Minimum two to three (2-3) year of experience in a clinical or scientific related discipline, preferably in oncology.

Nice To Haves

Associate's degree in a clinical or scientific related discipline desired, Bachelor's degree preferred.
Oncology research experience preferred.
EMR experience preferred.
SoCRA or ACRP certification preferred.

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.
Other duties as assigned