Oncology Clinical Research Nurse Solid Division F/T
2 months ago
Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community. Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.
The Oncology Clinical Research Nurse Solid Division is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies. The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the clinical trials.
A day in the life of a Clinical Research Nurse at Hackensack Meridian Health may include:
- Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
- Assures that all protocol revisions, informed consents, continuing reviews, serious adverse events are submitted to the appropriate IRB of record in a timely manner.
- Acts as liaison between principal investigators and sub-investigators on all regulatory issues and changes within the protocol.
- Interacts with regulatory specialists and principal investigators and sub-investigators on all regulatory issues and changes within the protocol.
- In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
- Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. Finalizes budget draft with budget coordinator.
- Recruits and evaluates potential study patients, and works with clinical research coordinator to schedule required appointments and interviews.
- Identifies the needs of the patient population served and modifies and delivers care that is specific to those needs (i.e., age, culture, hearing and/or visually impaired, etc.). This process includes communicating with the patient, parent, and/or primary caregiver(s) at their level (developmental/age, educational, literacy, etc.).
- Reviews medical records for potential study patients and ensures that medical records include documentation of all laboratory test results and procedures and progress of study patients, following guidelines set forth by the protocol sponsors.
- Instructs potential study patients, designated caregiver, physicians, nurse clinicians and other ancillary staff members involved in the care of the patient on aspects of patient¿s care, available trials, treatments and side effects.
- Assists investigator with consent process assuring study patients understand clinical trials and obtains written informed consent.
- Educates study patients concerning informed consent procedures, HIPAA authorization.
- Documents study patient¿s medical history including but not limited to past medical/surgical treatments, significant medical conditions, and medication history per protocol guidelines.
- Performs nursing assessments and monitors study patient¿s progress during clinical trials; Tracks study patient¿s response by documenting on toxicity flow sheet, medication flow sheet and nurses¿ progress notes.
- Maintains accurate, complete, up-to-date records on each patient participating in a clinical trial protocol in all applicable systems (i.e. electronic medical record, clinical trial management system, departmental and protocol specific databases).
- Evaluates and develops study patient education materials and gives study patient and/or designated caregiver instructions on drug administration and other medical information; creates study specific calendars for study patients.
- Plans for study patient¿s appropriate care under the direction of a physician or advanced practice nurse.
- Notifies principal investigator of any adverse events and serious adverse events, including evidence of drug toxicity or unexpected side effects.
- Reports all serious adverse events to sponsor and IRB of record according to established timelines.
- Coordinates research activiti
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Hackensack, New Jersey, United States Hackensack Meridian Health Full timeJob SummaryAt Hackensack Meridian Health, we are committed to delivering exceptional patient care and advancing the field of oncology through clinical research. We are seeking a highly skilled and dedicated Oncology Clinical Research Nurse to join our team in the Solid Division.Key ResponsibilitiesCoordinate and oversee clinical operations of clinical...
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Hackensack, New Jersey, United States HACKENSACK UNIVERSITY MED CNTR Full timeJob SummaryAt Hackensack University Medical Center, we are committed to providing exceptional patient care and advancing our mission to transform healthcare. As a Clinical Research Nurse in the Oncology Solid Division, you will play a critical role in coordinating and overseeing clinical operations of clinical trials, ensuring compliant patient care and...
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Hackensack, Minnesota, United States Hackensack Meridian Health Full timeTransforming Healthcare TogetherAt Hackensack Meridian Health, we're committed to delivering exceptional patient care and advancing our mission to transform healthcare. As a Clinical Research Nurse in our Oncology Solid Division, you'll play a vital role in coordinating and overseeing clinical operations of clinical trials, ensuring that our patients receive...
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Hackensack, United States HACKENSACK UNIVERSITY MED CNTR Full timeOur team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients live better, healthier lives and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. Its also about how we support one another and how...
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Hackensack, New Jersey, United States Hackensack Meridian Health Full timeJob SummaryWe are seeking a highly skilled Clinical Research Nurse to join our team in the Oncology Solid Division. The successful candidate will be responsible for coordinating and overseeing clinical operations of clinical trials, and participating in assessing, planning, implementing, and evaluating compliant patient care in clinical research studies.Key...
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Hackensack, United States Hackensack Meridian Health Full timeOur team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients live better, healthier lives and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. Its also about how we support one another and how...
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Hackensack, New Jersey, United States Hackensack Meridian Health Full timeJob SummaryWe are seeking a highly skilled Oncology Clinical Research Nurse to join our team in the Solid Division. The successful candidate will be responsible for coordinating and overseeing clinical operations of clinical trials, and will work under the general supervision of the principal investigator.Key ResponsibilitiesAssist the principal investigator...
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