Research Nurse (RN) Hematology/Oncology Full Time Days

East Tennessee Children's Hospital Association•Knoxville, TN

2d•Onsite

About The Position

Responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator, Research Center, and the Physicians. This role involves ensuring the scientific integrity of data and protecting the rights, safety, and well-being of patients enrolled in clinical trials. The Research Nurse will also maintain knowledge of research methodology, integrate ethics in practice, advocate for patients and families, and participate in self-evaluation of professional practice.

Requirements

Associates degree required.
Degree in Nursing, RN.
TN or Compact RN Licensure Required.
Minimum 3 years experience in nursing required.
Training/experience in research methods & statistics preferred.
Strong computer skills required.
Computer skills to include data entry and Internet research required.
Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals.

Nice To Haves

Bachelors degree preferred.
Bachelor of Science degree in Nursing preferred.
Certified Clinical Research Associate preferred.
Relative clinical experience preferred.

Responsibilities

Review research protocols prior to submittal to IRB.
Administratively manage clinical trials ensuring materials are available for physician review.
Assure that all patient pre-study material is available and reviewed by a physician.
Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials.
Discuss study protocols with patients and verify the informed consent documentation.
Ensure protocols and consents are updated and IRB informed of all changes.
Comply with IRB requirements regarding studies such as reporting adverse events.
Follow-up on abnormal lab values and ensure physician awareness.
Ensure continuing review of studies are submitted to IRB in a timely manner.
Assist physicians to ensure compliance with treatment plan for studies.
Communicate with research centers regarding all new patients (when applicable).
Collect, compile, and report data to the appropriate agency for patients on clinical trials.
Correspond to principal investigators regarding IRB decisions.
Assist in coordination of patients placed into follow-up.
Maintain knowledge of research methodology through educational programs.
Integrate ethics in all areas of practice.
Advocate for the protection, rights, and opportunities of patients and families.
Maintain current knowledge and competency in professional practice through participation in continuing education activities.
Participate in self-evaluation of his/her own practice in relation to professional practice standards and guidelines through activities such as peer review and solicitation of feedback from physicians and colleagues.
Collaborate with inter-professional teams, leaders, stakeholders, and others to facilitate positive outcomes for patients.
Willingly assume all other duties and responsibilities as necessary.
Consider factors related to safety, effectiveness, and cost in regard to expected outcomes.
Contribute to the budget process through planning and requests for human, financial and material resources necessary to meet identified needs.
Utilize hospital resources and time respectfully and accountably.