Oncology Research Nursing Specialist

1 week ago

New Brunswick, New Jersey, United States Vitalief Inc. Full time

WHY VITALIEF?

Vitalief is a pioneering Healthcare consulting firm dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Oncology Clinical Research Nurse to become part of our outstanding team (as a full-time, fully benefited employee) to support our mission and our clients' objectives to make a significant impact on patients' lives.

Benefits of working at Vitalief:

  • Contribute to our clients' goals of promoting scientific advancements that can transform patient care.
  • Our PEOPLE FIRST culture emphasizes both personal and professional development for all employees.
  • We foster an inclusive environment where innovation is encouraged.
  • Enjoy a healthy work-life balance with 20 PTO (Paid Time Off) days and 9 paid Holidays each year.
  • Additional benefits include company-paid life insurance, short and long-term disability coverage, a 401K retirement plan, and a variety of healthcare options.

Salary Range: Competitive, based on experience.

Work Location: This position requires on-site work 5 days a week, with the possibility of remote work one day per week after the initial training period.

Key Responsibilities:

  • Under the guidance of the Clinical Research Study Site Leader, this role involves supporting primarily Medical Oncology interventional studies (phases I to III) focusing on Solid Tumor, Lung, Head and Neck, Melanoma, and Neurology. The studies mainly involve drug and Biologic therapies.
  • Deliver high-quality, compassionate oncology nursing care while coordinating with the clinical team, investigators, and ancillary departments to ensure compliance with protocol requirements and adherence to Good Clinical Practice (GCP) guidelines.
  • Assist investigators in preparing and executing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management.
  • This role requires critical thinking, prioritization, and the ability to assertively communicate with physicians to ensure the accuracy of patient information relative to the study protocol.
  • On designated clinic days, the Nurse will see more patients, while on non-clinic days, administrative tasks such as patient documentation and order verification will be performed.
  • Collaborate with the Protocol Activation office to initiate and activate new clinical trial protocols using the Oncore Study-startup task list.
  • Review patient charts and medical histories to confirm eligibility for protocols and obtain necessary source documents.
  • Demonstrate knowledge of core tasks, including timely reporting of Serious Adverse Events (SAE), accessing protocol attachments, and managing patient study calendars.

Required Qualifications:

  • Graduate from an accredited nursing program with a valid nursing license in New Jersey.
  • Bachelor of Science in Nursing (BSN) is required.
  • A minimum of 2 years of nursing experience in a hospital environment.
  • At least 1 year of experience in an Oncology specialty area.
  • Experience in a clinical research role is advantageous but not mandatory, as training will be provided.
  • Strong critical thinking skills and the ability to communicate effectively with other departments.
  • Proficient in document management and familiar with Microsoft Office applications.
  • Detail-oriented and able to thrive in a dynamic, academic, and diverse setting.
  • Proactive and eager to learn, with a willingness to ask questions.
  • Familiarity with clinical trial management systems and medical records databases is preferred.

PHYSICAL DEMANDS: This role requires standing, sitting, walking, visual perception, and effective communication. Ability to lift up to 20 lbs.

IMPORTANT NOTE: Vitalief collaborates with major medical centers and academic institutions, which may require annual vaccinations and successful completion of a Tuberculin Skin Test (TST).

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