Clinical Research Coordinator - Medical Office

Overview:

$2,500 Sign On Bonus!
Clinical Research Coordinator
Willamette Valley Cancer Institute and Research Center, located in Eugene, has an exciting opportunity for a Clinical Research Coordinator. This position is open to both non-clinical applicants (CRC), as well as clinical (RN CRC).
Salary Range:
CRC - $50,000-$90,000
RN II CRC - $59,576-101,255
Employment Type : Full Time - 40hr/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.
• 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.

• May disburse investigational drug and provide patient teaching regarding administration.
• Maintains investigational drug accountability.

• Minimum one to three (1-3 ) years of experience in a clinical or scientific related discipline, preferably in oncology.
• Oncology research experience preferred.
• EMR experience preferred.
• SoCRA or ACRP certification preferred.

• Associate's degree in nursing, BSN degree preferred.
• RN License in OR REQUIRED
• Minimum one to three (1-3) 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.