Comprehensive Cancer Centers of Nevada
Clinical Research Coordinator - Twain
Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, us, 89105
Overview
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 give many of our patients the opportunity to receive newly developed treatments or investigational drugs not yet available outside the study.
CCCN develops and conducts more than 170 Phase I, II and 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 Full‑time Clinical Research Coordinator, on‑site at our Twain clinic in Las Vegas, Nevada. The role is responsible for the collection, coordination, processing, and quality control of clinical trial data.
Scope The Coordinator supports the management and coordination of tasks for multiple clinical research studies, including screening patients for eligibility and participating in the subject’s study visits and required activities per protocol. Duties include ensuring protocol compliance, participating in informed consent, performing ongoing assessments and documentation in collaboration with physicians and other providers, undertaking required training and education, and maintaining compliance with US Oncology Research, Inc. (USOR) SOP, GCP and applicable federal, state, and local regulations.
Responsibilities
Enlist, maintain, and assure protocol compliance for all patients on clinical trials.
Collaborate with physicians to determine eligibility of patients for clinical trials.
Practice in compliance with SOP, GCP, and applicable federal, state, and local regulations.
Screen potential patients, present trial concepts and details, participate in informed consent, and enroll patients.
Coordinate patient care in compliance with protocol requirements; may disburse investigational drugs and provide patient teaching; maintain drug accountability.
Review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug; thoroughly document findings.
Collect, document, enter, and report data accurately and timely; schedule and participate in monitoring and auditing activities.
Maintain regulatory documents by SOP and applicable regulations.
Participate in required training and education programs; educate clinic staff regarding clinical research.
Collaboration with Research Site Leader in study selection (when applicable).
Work directly with other research bases and/or sponsors (when needed).
Provide a safe environment for patients, families, and clinical staff through compliance with all federal, state, and professional regulatory standards; maintain strict patient confidentiality per HIPAA.
Minimum Qualifications
High school diploma or equivalent.
Associate’s degree in a clinical or scientific‑related discipline required; Bachelor’s Degree preferred.
Minimum one (1) year medical office experience, oncology or clinical research preferred.
SoCRA or ACRP certification preferred.
Equal Opportunity Statement 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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CCCN develops and conducts more than 170 Phase I, II and 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 Full‑time Clinical Research Coordinator, on‑site at our Twain clinic in Las Vegas, Nevada. The role is responsible for the collection, coordination, processing, and quality control of clinical trial data.
Scope The Coordinator supports the management and coordination of tasks for multiple clinical research studies, including screening patients for eligibility and participating in the subject’s study visits and required activities per protocol. Duties include ensuring protocol compliance, participating in informed consent, performing ongoing assessments and documentation in collaboration with physicians and other providers, undertaking required training and education, and maintaining compliance with US Oncology Research, Inc. (USOR) SOP, GCP and applicable federal, state, and local regulations.
Responsibilities
Enlist, maintain, and assure protocol compliance for all patients on clinical trials.
Collaborate with physicians to determine eligibility of patients for clinical trials.
Practice in compliance with SOP, GCP, and applicable federal, state, and local regulations.
Screen potential patients, present trial concepts and details, participate in informed consent, and enroll patients.
Coordinate patient care in compliance with protocol requirements; may disburse investigational drugs and provide patient teaching; maintain drug accountability.
Review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug; thoroughly document findings.
Collect, document, enter, and report data accurately and timely; schedule and participate in monitoring and auditing activities.
Maintain regulatory documents by SOP and applicable regulations.
Participate in required training and education programs; educate clinic staff regarding clinical research.
Collaboration with Research Site Leader in study selection (when applicable).
Work directly with other research bases and/or sponsors (when needed).
Provide a safe environment for patients, families, and clinical staff through compliance with all federal, state, and professional regulatory standards; maintain strict patient confidentiality per HIPAA.
Minimum Qualifications
High school diploma or equivalent.
Associate’s degree in a clinical or scientific‑related discipline required; Bachelor’s Degree preferred.
Minimum one (1) year medical office experience, oncology or clinical research preferred.
SoCRA or ACRP certification preferred.
Equal Opportunity Statement 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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