Clinical Research Coordinator, RN - F/T career at Virginia Cancer Specialists in Fairfax

Virginia Cancer Specialists is currently interviewing Clinical Research Coordinator, RN - F/T on Wed, 01 Jan 2014 17:53:59 GMT. Coordinator, Nurse in our Fairfax, VA. office. Week day hours, Monday-Friday. Scope of position: Under direct supervision of a physician and nurse (if...

Clinical Research Coordinator, RN - F/T

Location: Fairfax Virginia

Description: Virginia Cancer Specialists is currently interviewing Clinical Research Coordinator, RN - F/T right now, this career will be placed in Virginia. For complete informations about this career opportunity please give attention to these descriptions. Virginia Cancer Specialists, affiliated with McKesson Specialty Health and US Oncology, a leader in cancer care, has an exciting full time opportunity for an Clinical Research Coordinator, Nurse in our Fairfax, VA. office. Week day hours, Monday-Friday.

Scope of position:
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 det! ermining 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.

ESSENTIAL DUTIES AND 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 reporti! ng. Schedules and participates in monitoring and auditing activities.
Maintains regulatory documents in accordance with USOR SOP and applicable regulations.
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.
RN with Oncology experience and previous clinical research experience with Phase I Clinical Trials preferred.
Possible local travel to other locations.
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If you were eligible to this career, please email us your resume, with salary requirements and a resume to Virginia Cancer Specialists.

If you interested on this career just click on the Apply button, you will be redirected to the official! website

This career starts available on: Wed, 01 Jan 2014 17:53:59 GMT

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