The RN Oncology Research Coordinator is a proactive member of an interdisciplinary team of licensed and unlicensed care givers who ensure that patients, families and significant others receive individualized high quality, safe patient care. It is expected that all RN Clinical Nurses - are licensed, knowledgeable and uphold the practice of nursing as outlined by the Georgia Professional Nurse Practice Act and implements the Scope of Practice and Code of Ethics Standards put forth by the American Nurses Association.
Schedule:Full Time
Shift: Day Shift
Level: 6+ years of experience
Success Profile Find out what it takes to succeed as a RN Oncology Research Coordinator:
Collaborative
Time Efficient
Organized
Critical Thinker
Attention to Detail
Compassionate
Benefits that Reflect Your Contributions
Your Pay A compensation program designed for fair and equitable pay.
Your Future Secure your future with plans that also include an employer match. Plans and guidance for the future.
Your Wellness Traditional healthcare benefits combined with progressive wellness programs to help you be your best self!.
Your Joy Special and unique benefits and programs ensuring a balanced life and a workplace culture built on trust.
Job Details
Facility: Kennestone Hospital
Job Summary:
The Research Coordinator has general responsibility for managing clinical trials for the Clinical Trials Office of the WellStar Health System. This includes responsibility for identifying potential study patients; ascertaining patient eligibility for clinical trials; coordinating, evaluating, and following patients in clinical trials; coordinating therapy initiation and continuation; taking call for issues related to clinical trials; completing and filing necessary forms with internal and external departments and agencies as necessary; and maintaining records for patients enrolled in clinical trials.
Core Responsibilities and Essential Functions:
Coordinates all facets of patient involvement in clinical trials. - Conducts all aspects of clinical trial, including consenting, using Good Clinical Practice, FDA, and Institutional guidelines. - Reviews patient chart for eligibility requirements and enrolls patient according to protocol guidelines. - Communicates with physician/office staff regarding scheduling protocol specific requirements. - Attends patient visits and gathers protocol-specific information when required. - Communicates drug doses, protocol requirements and modifications to physician and office staff as appropriate. - Coordinates dispersement of protocol provided drug therapy. - Ensures that Investigation Product chain-of-custody practices are instituted and documented. Maintains accurate records for patients enrolled on clinical trials. - Communicates effectively with Research Assistants and other research staff. - Gathers appropriate source documentation - Submits required documentation within designated time frame. - Provides proper documentation of eligibility, treatment and follow-up requirements. - Provides accurate research information to physicians and sponsors. - Maintains a current chart on each protocol patient. - Enters patient visits into clinical trial database. Ensures regulatory guidelines are followed. - Prepares research charts for monitoring visits and audits and assists with visits as required. - Follows guidelines and timelines for reporting Adverse Events and Deviations. - Maintains current protocol with revisions, amendments and current IRB approved informed consent. Ensures clinical trial and sponsor-required training is completed. - Ensures that all training related to start-up of a clinical trial is accomplished, including attending Investigator Meetings when required. - Ensures that ongoing training during the course of a clinical trial is completed. - Facilitates ongoing training for other team members, including investigators. - Maintains current Human Research Participant Protection and Hazardous Material training. Assists with other departmental functions. - Attends committee meetings as required. - Attends functional team meetings and disseminates information. - Assists with regulatory and billing functions, when required. - Responsible for additional projects, as directed by the manager.
Required Minimum Education:
Graduate from an approved school of nursing. Required and Bachelor's Degree BSN Preferred
Minimum 5 years of experience as a nurse; Required and Hospital experience Preferred and Critical Care experience Preferred and Research experience Preferred
Required Minimum Skills:
Strong computer skills; good oral and written communication skills; excellent interpersonal and organization skills.
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Mission, Vision & Values At a time when the healthcare industry is changing rapidly, Wellstar remains committed to exceeding patients' and team members' expectations, while transforming healthcare delivery.
Our Mission To enhance the health and well-being of every person we serve.
Our Vision Deliver worldclass health care to every person, every time.
