Registered Nurse Clinical Research - Twain

Registered Nurse Clinical Research - Twain 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 help uncover new treatment options and allow many 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, ensuring 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 Collaborate with physicians and other providers to screen potential patients for eligibility Present trial concepts and details to the patients, participate in the informed consent process, and enroll patients in clinical trials Coordinate patient care in compliance with protocol requirements; dispense investigational drugs and provide patient teaching regarding the administration Maintain investigational drug accountability; review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug, and thoroughly document all findings Review protocol-specific billing guides and submit billing information to appropriate personnel Collaborate with study team on subject recruitment and study enrollment goals; work with the team to determine effective strategies for promoting/recruiting research participants and retaining participants in long‑term clinical trials Provide clinical services as required including patient assessments Assist with the collection and maintenance of regulatory documents by USOR SOP and applicable regulations Potentially collaborate with Research Site Leader in the study selection process Potentially participate in scheduling monitoring and auditing visits as well as interact with monitors/auditors while onsite Participate in required training and education of staff and patients Assist with the preparation of orders by physicians to assure that protocol compliance is maintained Communicate with the physician regarding study requirements, need for dose modification, and adverse event reporting Potentially be responsible for basic clinical assessments Qualifications Graduate from an accredited program for nursing education (BSN preferred) Current licensure as a Registered Nurse in Nevada Current BLCS or ACLS certification OCN, SoCRA or ACRP certification preferred Knowledge of medical terminology, nursing assessment, clinical trials, and GCP concepts Preferred: three years of clinical research experience Experience in Microsoft Office 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 Excellent communication, time management, and organizational skills, and a strong ability to multi‑task High level of attention to detail Ability 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. 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. #J-18808-Ljbffr US Oncology Network-wide Career Opportunities