Comprehensive Cancer Centers of Nevada
Clinical Research Coordinator - Twain
Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, us, 89105
Clinical Research Coordinator - Twain
Location:
Las Vegas, Nevada
Research
Comprehensive Cancer Centers of Nevada (CCCN)
Zip: 35941
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, 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 A full-time, on‑site Clinical Research Coordinator at our Twain clinic in Las Vegas, Nevada. This person is responsible for the collection, coordination, processing, and quality control of clinical trial data.
Scope Responsible for supporting 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 for all patients enrolled in the trial, performing ongoing assessments and documentation in collaboration with physicians and other providers, and supporting compliance with SOPs, GCP, and applicable regulations.
Responsibilities
Under direct supervision of a physician and nurse, enlists, maintains, and assures protocol compliance for all patients on clinical trials.
Collaborates with physicians in determining eligibility of patients for clinical trials.
Ensures site research quality by practicing compliance with SOPs, GCP, and applicable regulations.
Screen potential patients for protocol eligibility; presents trial concepts, participates in informed consent process, and enrolls patients in protocol.
Coordinates patient care in compliance with protocol requirements; may disburse investigational drugs and provide patient teaching regarding administration. Maintains investigational drug accountability.
Reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug and 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 by SOPs 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 research sites and/or sponsors.
Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards; maintains strict patient confidentiality according to HIPAA regulations.
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 of medical office experience, oncology or clinical research preferred.
SoCRA or ACRP certification preferred.
Benefits & Application Successful candidates will thrive in a fast‑paced, rapidly changing environment and have a passion for caring for their patients. We offer excellent benefits, a team environment, professional development, and the chance to be part of a nationwide network dedicated to fighting cancer.
Ready for your next career challenge? If you possess the above qualifications and a desire to make a difference, we invite you to submit your resume and apply. To apply, please click 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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Las Vegas, Nevada
Research
Comprehensive Cancer Centers of Nevada (CCCN)
Zip: 35941
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, 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 A full-time, on‑site Clinical Research Coordinator at our Twain clinic in Las Vegas, Nevada. This person is responsible for the collection, coordination, processing, and quality control of clinical trial data.
Scope Responsible for supporting 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 for all patients enrolled in the trial, performing ongoing assessments and documentation in collaboration with physicians and other providers, and supporting compliance with SOPs, GCP, and applicable regulations.
Responsibilities
Under direct supervision of a physician and nurse, enlists, maintains, and assures protocol compliance for all patients on clinical trials.
Collaborates with physicians in determining eligibility of patients for clinical trials.
Ensures site research quality by practicing compliance with SOPs, GCP, and applicable regulations.
Screen potential patients for protocol eligibility; presents trial concepts, participates in informed consent process, and enrolls patients in protocol.
Coordinates patient care in compliance with protocol requirements; may disburse investigational drugs and provide patient teaching regarding administration. Maintains investigational drug accountability.
Reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug and 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 by SOPs 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 research sites and/or sponsors.
Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards; maintains strict patient confidentiality according to HIPAA regulations.
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 of medical office experience, oncology or clinical research preferred.
SoCRA or ACRP certification preferred.
Benefits & Application Successful candidates will thrive in a fast‑paced, rapidly changing environment and have a passion for caring for their patients. We offer excellent benefits, a team environment, professional development, and the chance to be part of a nationwide network dedicated to fighting cancer.
Ready for your next career challenge? If you possess the above qualifications and a desire to make a difference, we invite you to submit your resume and apply. To apply, please click 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.
#J-18808-Ljbffr