Registered Nurse RN Clinical Research Oncology
Company: Drug Information Association Inc
Location: Sun City
Posted on: May 6, 2022
Internal Number: R77245
Sun City, Arizona
MDA Research ATU
* 10K-15k Sign On Bonus Offered*
Nursing careers are better at Banner Health. We are committed to
developing the careers of our team members. We care about you, your
nursing career today and your future. If you???re looking to
leverage your abilities ??? apply today.??
Those who have joined the Banner mission come from all walks of
life, united by the common goal: Make health care easier, so life
can be better. If changing health care for the better sounds like
something you want to be part of, we want to hear from you.
Banner MD Anderson Cancer Center Clinical Trials Office is the
oncology service line for Banner Research. The department operates
in Banner MD Anderson Cancer Center and Banner Gateway Medical
Center. The department conducts Phases I-III treatment clinical
trials covering all disease groups with the goal to provide support
to the physician investigators and to provide trial treatment
options to the patients in a safe and ethical manner, while
ensuring compliance to the FDA and institutional regulations.
Schedule: Monday - Friday no weekends, no holidays! Flexible
schedule option of 5's or 410's a week.
* Sign On Bonus Offered* Requires 24 month commitment
* 10K for 2+ years of oncology OR research experience
* 15K for 2+ years of oncology AND research experience
If you are a New Graduate Nurse with less than 12 months of
experience, please visit the main job search page and under the Job
Type filter, select New Nurse Experience.
Since 1970, Banner Boswell Medical Center has provided exceptional
care to the people in the northwest area of metropolitan Phoenix.
Today, our 501-bed acute-care hospital is recognized by U.S. News
and World Report as one of Phoenix's Best Hospitals and offers a
full range of acute care services, including cardiology, oncology,
orthopedics, neurology, surgery, rehabilitation, emergency, stroke,
intensive care, pulmonary, urology, wound management and sleep
disorders. We've earned the Gold Seal of Approval from The Joint
Commission for Primary Stroke Centers. We're also in the nation's
top five percent for preventing mortality and complications.
This position provides coordination of investigational and research
protocols. Coordinates operational aspects of research projects
including project preparation, subject recruitment, protocol
execution, data collection, and coordination and database
1. Promotes research study initiation and review. Acts as the
project representative and professional resource for coordination
of staff, sponsors, research institutions, contract research
organizations, regulatory agencies, and involved institutional
departments. Reads and evaluates clinical research protocols.
Attends departmental, committee, and sponsor meetings for the
purpose of gathering new or revised information concerning existing
or potential clinical research projects.
2. Ensures that the clinical research staff and/or students conduct
the clinical aspects of the projects appropriately and adhere to
the clinical trial schedule, which may include: maintaining,
dispensing and recording drug and medical device supplies according
to regulations; assisting in obtaining informed consent from
project participants; assisting in the development and
implementation of case report forms; instructing volunteers on
protocol requirements and explaining procedures and consent forms;
performing research patient registration; ensuring that clinical
research staff conduct the clinical aspects of the projects
appropriately and adhere to the schedule of the clinical trials;
serving as an advocate for the research participant, assisting them
through the research process; and/or, performing other related
3. Develops and maintains regulatory and legal documents per
guidelines and regulations of the research/study sponsor and the
participating institution per IRB, FDA, PHA and other applicable
regulatory agencies. Assists in annual reporting to Federal
agencies as required.
4. Performs accurate data collection and reporting according to
protocol requirements and completes applicable forms and/or other
required reports in a timely manner. Facilitates and conducts site
reviews with sponsors and other related agencies for the purpose of
evaluating the accuracy and quality of the collected data. Develops
and implements patient tracking and follow-up systems. Coordinates
with participating physicians offices and staff for patient
5. Assists in educating patients about research studies and in
obtaining informed consent from project participants. Develops and
maintains educational tools, educates research team members and
assists staff in the conduct of the investigational therapy.
Performs medical record reviews. Assists with patient recruitment,
screening, diagnostics, treatment and education. Utilizes clinical
knowledge and assessment skills necessary to evaluate, report and
record accurate medical information, including responses to
6. Assists in the development and maintenance of budget and/or
contract agreements. Follows policy requirements for reporting
patient enrollment in an effort to ensure compliance with billing.
Assists in the development of accounting reports and in
coordination of billing systems.
7. Coordinates and safely implements research activities through
interactions with research staff, internal and external
investigators, study sponsors and Institutional Review Board
8. Participates in the development of clinical research protocols.
Performs accurate and timely data collection and reporting
according to protocol requirements. Facilitates and conducts site
reviews by sponsors and other related agencies for the purpose of
monitoring the accuracy and quality of the collected data. May
hire, train, conduct performance reviews, and direct the workflow
for the department staff.
9. This position provides collaboration with various clinical and
administrative positions, as well as research staff. Maintains
primary facility assignment but may be asked to collaborate
elsewhere either inside or outside of system. Conducts
presentations to academic, professional and layperson
Must possess a thorough knowledge of nursing and healthcare as
normally demonstrated through the completion of a Bachelors Degree
Requires a current Registered Nurse (R.N.) license. Possession of
or ability to obtain a Clinical Research Coordinator Certification
(CRCC) within a reasonable timeframe.
Experience typically gained through two years clinical research
experience or experience related to clinical area in which research
study is based. Previous relevant experience working in a clinical
research setting. Knowledge of medical and clinical terminology.
Excellent organizational and task management skills and the ability
to maintain confidentiality of patient and study information.
Ability to maintain knowledge of Federal and State regulations
governing practice as well as Institute policies and procedures
related to medical and nursing practice. Excellent human relations,
organizational and communication skills.
Ability to conduct computer-based literature searches is
Master???s Degree or advanced certificate degrees preferred.
Regulatory knowledge regarding the conduct of clinical research or
health care operations is preferred.
Additional related education and/or experience preferred.
Keywords: Drug Information Association Inc, Sun City , Registered Nurse RN Clinical Research Oncology, Healthcare , Sun City, Arizona
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