Oncology Associate Clinical Research Coordinator

Oncology Associate Clinical Research Coordinator page is loaded## Oncology Associate Clinical Research Coordinator locations:
Banner Gateway Med Ctr (1900 N Higley Rd) time type:
Full time posted on:
Posted Todayjob requisition :
R4429774
** Primary City/State:
** Gilbert, Arizona
** Department Name:
** BMDACC Gateway Oncology-Rsrch
*
* Work Shift:

** Day
* * Job Category:
** Research
* * 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.

As an
** Associate Clinical Research Coordinator in Oncology,
** you will play a vital role in supporting the conduct of clinical research studies by managing key operational tasks and ensuring accurate data collection and entry. Working under the guidance of a Clinical Research Coordinator or RN Specialist, you will coordinate study protocols, schedule appointments and procedures, and maintain ongoing communication with study participants. Your responsibilities will include screening and enrolling participants, verifying eligibility, obtaining informed consent, and reviewing medical histories.

You will also maintain patient calendars, manage research databases, perform quality reviews, and prepare and submit reports, all while ensuring compliance with study protocols and regulatory requirements. This is a unique opportunity where you can
** apply your established research or oncology experience
** to groundbreaking oncology research that directly impacts patient care and advances medical knowledge,
* join a team where your work truly makes a difference.
*** 2yrs of Clinical Research Required
***
* Schedule:

*
* ** Monday through Friday, 8am-4:30pm
** Banner Alzheimer's Institute (BAI) was established in 2006 as Banner Health's first Center of Excellence. Banner Sun Research Health Institute (BSHRI) was founded in 1986. Our team is uniquely, passionately, and strategically committed to ending Alzheimer's disease and other neurodegenerative disorders without losing another generation and to providing an unparalleled model of care for families facing this devastating disease. Banner Research is committed to improving people's lives through comprehensive patient care and advances that capitalize on the best biomedical research.

We intend to make a transformational difference in Alzheimer's disease and other neurodegenerative disorders research and care.

POSITION SUMMARY This position is responsible for providing research clinical conduct and data collection and entry support for clinical research studies.  Duties include handling key operational functions for research studies and abstracting relevant research related data from medical records and source documents, populating, and coordinating use of research data bases and data sources, participant consenting, screening, enrollment, quality review, training, report production, and submission of collected research data.

CORE FUNCTIONS
1. Under the direction of the RN Specialist, Clinical Research Coordinator or principal investigator, coordinates research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
2. Maintains patient calendars, screening, and enrollment information utilizing departmental databases/tools to ensure compliance with protocol requirements.
3. Completes initial intake on participants for research studies. Determines participant eligibility based on study specific criteria. Verifies that patients have completed appropriate registration materials and maintains related records and information. Obtains and reviews relevant medical history with participants.
4. Accountable for completing entire informed consent process, which includes proper…