Comprehensive Cancer Centers of Nevada
Research Data Coordinator - Twain
Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, us, 89105
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Research Data Coordinator - Twain
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Research Data Coordinator - Twain
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Research Data Coordinator - Twain
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Las Vegas, Nevada Research Comprehensive Cancer Centers of Nevada 34479
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 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
Comprehensive Cancer Centers of Nevada has an exciting opportunity for a Clinical Research Data Coordinator at our Twain office in Las Vegas, Nevada. This person is responsible for the collection, coordination, processing, and quality control of clinical trial data.
Scope
Under general supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data, maintaining research protocol and other research files as applicable. Works with clinical staff to meet data entry timelines and communicate any concerns about the data. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice (GCP) and all applicable federal state and local regulations. Supports and adheres to the US Oncology Compliance Program to include the Code of Ethics and Business Standards.
Responsibilities
Key Responsibilities
Extrapolate data from source records into case report forms for all patient visits and ensure timely data submission in accordance with USOR SOPs. Responsible for resolving queries, communicating concerns or questions about data to clinical staff and or research management. Utilizes USOR clinical trial management system to access research forms and keep current all applicable patient reporting and tracking functions including but not limited to subject CRF Binders/Folders. Maintains research records in a confidential manner according to practice policies sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations. Actively participates in sponsor monitoring and auditing visits, ensuring that all data and queries are entered and resolved in accordance with USOR and sponsor requirements. Assist with ordering and maintaining research supplies. Assist with scheduling patient follow up appointments and/or procedures required to maintain protocol compliance. Assist with collecting and processing of specimens, imaging documents, and other items required for research purposes.
Qualifications
Minimum Job Qualifications (Knowledge, Skills, & Abilities):
Education/Training -
High School Diploma required Associates Degree strongly desired; Bachelor's Degree preferred 0-3 Years work experience Some medical office experience required, preferably oncology
Business Experience -
Experience in Microsoft Office Experience with computer data entry and database management Experience in clinical research desired High computer literacy required
Specialized Knowledge/Skills -
Excellent written and oral communication skills Excellent multi-tasking skills High attention to detail and accuracy Ability to independently organize, prioritize, and make decisions Knowledgeable of medical terminology
Working Conditions
Environment (Office, warehouse, etc.) -
Traditional office environment. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.
Physical Requirements (Lifting, Standing, Etc.) -
Large percent of time performing computer-based work is required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.
Ready For Your Next Career Challenge? Wed 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.
Apply
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Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
Research Data Coordinator - Twain
role at
Comprehensive Cancer Centers of Nevada Join to apply for the
Research Data Coordinator - Twain
role at
Comprehensive Cancer Centers of Nevada Get AI-powered advice on this job and more exclusive features. Back
Research Data Coordinator - Twain
JOB_DESCRIPTION.SHARE.HTML
CAROUSEL_PARAGRAPH
JOB_DESCRIPTION.SHARE.HTML
Las Vegas, Nevada Research Comprehensive Cancer Centers of Nevada 34479
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 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
Comprehensive Cancer Centers of Nevada has an exciting opportunity for a Clinical Research Data Coordinator at our Twain office in Las Vegas, Nevada. This person is responsible for the collection, coordination, processing, and quality control of clinical trial data.
Scope
Under general supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data, maintaining research protocol and other research files as applicable. Works with clinical staff to meet data entry timelines and communicate any concerns about the data. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice (GCP) and all applicable federal state and local regulations. Supports and adheres to the US Oncology Compliance Program to include the Code of Ethics and Business Standards.
Responsibilities
Key Responsibilities
Extrapolate data from source records into case report forms for all patient visits and ensure timely data submission in accordance with USOR SOPs. Responsible for resolving queries, communicating concerns or questions about data to clinical staff and or research management. Utilizes USOR clinical trial management system to access research forms and keep current all applicable patient reporting and tracking functions including but not limited to subject CRF Binders/Folders. Maintains research records in a confidential manner according to practice policies sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations. Actively participates in sponsor monitoring and auditing visits, ensuring that all data and queries are entered and resolved in accordance with USOR and sponsor requirements. Assist with ordering and maintaining research supplies. Assist with scheduling patient follow up appointments and/or procedures required to maintain protocol compliance. Assist with collecting and processing of specimens, imaging documents, and other items required for research purposes.
Qualifications
Minimum Job Qualifications (Knowledge, Skills, & Abilities):
Education/Training -
High School Diploma required Associates Degree strongly desired; Bachelor's Degree preferred 0-3 Years work experience Some medical office experience required, preferably oncology
Business Experience -
Experience in Microsoft Office Experience with computer data entry and database management Experience in clinical research desired High computer literacy required
Specialized Knowledge/Skills -
Excellent written and oral communication skills Excellent multi-tasking skills High attention to detail and accuracy Ability to independently organize, prioritize, and make decisions Knowledgeable of medical terminology
Working Conditions
Environment (Office, warehouse, etc.) -
Traditional office environment. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.
Physical Requirements (Lifting, Standing, Etc.) -
Large percent of time performing computer-based work is required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.
Ready For Your Next Career Challenge? Wed 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.
Apply
JOB_DESCRIPTION.SHARE.HTML
CAROUSEL_PARAGRAPH
JOB_DESCRIPTION.SHARE.HTML
Seniority level
Seniority level
Entry level Employment type
Employment type
Full-time Job function
Job function
Information Technology Industries
Hospitals and Health Care Referrals increase your chances of interviewing at Comprehensive Cancer Centers of Nevada by 2x Sign in to set job alerts for Data Coordinator roles.
Las Vegas, NV $50,000.00-$55,000.00 3 weeks ago Henderson, NV $70,000.00-$80,000.00 21 hours ago Las Vegas, NV $65,000.00-$85,000.00 4 days ago Online Data Analyst - Fully Remote Position
Intake Coordinator / Administrative Assistant
Online Data Analyst - Fully Remote Position
Data Visualization Analyst II- Research and Development
Las Vegas, NV $125,000.00-$160,000.00 22 hours ago Business Systems Analyst I/II (Plant Operations)
Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr