Position Summary
Company 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 professional are encouraged to join us.
Career Opportunity:
Comprehensive Cancer Centers of Nevada has an exciting opportunity for a Clinical Research Data Coordinator at our Viking office in Las Vegas, Nevada. This person is responsible for the collection, coordination, processing and quality control of clinical trial data.
The essential functions for the Clinical Research Data Coordinator include the following:
- Maintains research protocol information, regulatory documents and other research files as applicable
- Under general supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data
- Extrapolates data, completes case report forms, and ensures timely data submission
- Utilizes Clinical Trial Management System (CTMS) and electronic data capturing systems (eDC) to access research forms and keeps current all applicable patient reporting and tracking functions
- Actively prepares for and participates in monitoring and auditing activities
- Assists in ensuring that all queries are resolved in a timely manner in accordance with and sponsor requirements
- Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations
- Act as a liaison between physicians, monitors, CRCs and regulatory staff
- Maintains compliance with FDA, DCP and IHC guidelines
The ideal candidate will have the following background and experience:
- High school diploma or equivalent
- Associate's degree strongly desired, Bachelor’s Degree preferred
- Minimum one year medical office experience, oncology or clinical research preferred
- SoCRA or ACRP certification preferred
Successful candidates will thrive in a fast paced, rapidly changing environment and have a passion for working with and providing assistance to 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 fight the war against cancer. To apply please click on the Apply Now button.
Category: Clinical
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.