Registered Nurse Clinical Research - Twain

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Registered Nurse Clinical Research - Twain

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• Las Vegas, Nevada
• Research
• Comprehensive Cancer Centers of Nevada
• 39573
  
  

Overview

Job Description

Comprehensive Cancer Centers of Nevada (CCCN) is dedicated to advancing cancer care by leading and participating in many clinical research studies in Nevada that test the safety and efficiency of new or modified treatments in cancer patients. These trials are important because they help uncover new treatment options and allow many of our patients to receive newly developed treatments or investigational drugs not yet available outside the study.

CCCN develops and conducts more than 170 Phase I, Phase II, and Phase III clinical research trials each year including genitourinary and gastrointestinal cancer treatments, radiation clinical trials, breast cancer, and skin cancer. Motivated, caring professionals are encouraged to join us.

Career Opportunity

Comprehensive Cancer Centers of Nevada has an exciting opportunity for a Phase I RN - Clinical Research Coordinator at our Twain clinic in Las Vegas, Nevada. This person is responsible for the screening, enrollment, and maintenance of patients in clinical trials.

Scope

Duties include assuring protocol compliance for all patients on trial, participation in the consent process, collaboration with physicians and other providers ongoing assessments for changes in condition and adverse events, accurate and timely documentation/data entry, participation in education and training of other 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 the US Oncology Compliance Program, including the Code of Ethics Business Standards.

Responsibilities

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Collaborates with physicians and other providers to screen potential patients for eligibility
• Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients in clinical trials
• Coordinates patient care in compliance with protocol requirements; dispenses investigational drugs and provides patient teaching regarding the administration
• Maintains investigational drug accountability; in collaboration with the physician and other providers, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug and thoroughly documents all findings
• Responsible for reviewing protocol-specific billing guides and submitting billing information to appropriate personnel
• Collaborates with study team on subject recruitment and study enrollment goals; works with the team to determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials
• Provides clinical services as required including patient assessments
• Assists with the collection and maintenance of regulatory documents by USOR SOP and applicable regulations
• May collaborate with Research Site Leader in the study selection process
• May participate in scheduling monitoring and auditing visits as well as interact with the monitors/auditors while onsite
• Participates in required training and education of staff and patients
• Assists with the preparation of orders by physicians to assure that protocol compliance is maintained
• Communicates with the physician regarding study requirements, need for dose modification, and adverse event reporting
• May be responsible for basic clinical assessments
  
  

Qualifications

MINIMUM QUALIFICATIONS:

• Graduate from an accredited program for nursing education required (BSN preferred)
• Current licensure as a Registered Nurse in Nevada required
• Current BLCS or ACLS certification required
• OCN, SoCRA or ACRP certification preferred
• Knowledge of medical terminology, nursing assessment, clinical trials, and GCP concepts
• Three years of clinical research experience preferred
• Experience in Microsoft Office required
• Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents
• Ability to work independently, organize, prioritize, and follow through with results
• Must have excellent communication, time management, and organizational skills, and a strong ability to multi-task
• Must have a high level of attention to detail
• Must be able to work in a fast-paced environment
  
  

Successful candidates will thrive in a fast-paced, rapidly changing environment and have a passion for caring for their patients.

Ready For Your Next Career Challenge? We’d Love to Hear from You!

If you possess the above qualifications and a desire to make a difference, we invite you to submit your resume and apply. In addition to a great career opportunity, we offer excellent benefits, a team environment, professional development, and the chance to be part of a nationwide network dedicated to fighting the war against cancer. To apply please click on the “Apply” link.

The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status. This employer participates in E-Verify.

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