Oncology Research Nursing Specialist

1 week ago

New Brunswick, New Jersey, United States Vitalief Full time
Position Overview

Join Vitalief's Mission
Vitalief is a pioneering healthcare consulting firm dedicated to enhancing research and transforming clinical trials. We are currently in search of a skilled and passionate Oncology Clinical Research Nurse to become an integral part of our outstanding team. This role offers a unique opportunity for experienced oncology nurses looking to transition into a fulfilling career within the clinical research field.

Why Choose Vitalief?

  • Contribute to groundbreaking scientific advancements that can significantly improve patient outcomes.
  • Embrace a People First culture that emphasizes both personal and professional development for all team members.
  • Participate in a collaborative environment that fosters innovation and encourages diverse perspectives.
  • Enjoy a healthy work-life balance with generous paid time off and holidays.
  • Benefit from comprehensive health plans, company-paid life insurance, and a robust retirement program.

Compensation: Competitive salary based on experience.

Work Environment: This position requires on-site work five days a week, with the potential for remote work after an initial training period.

Key Responsibilities:

  • Assist the Clinical Research Study Site Leader in managing medical oncology interventional studies across various phases, focusing on solid tumors and other specified areas.
  • Deliver compassionate and high-quality oncology nursing care while coordinating with clinical teams, investigators, and relevant departments to ensure compliance with study protocols and Good Clinical Practice (GCP) standards.
  • Support investigators in the preparation and execution of clinical trials, including participant screening, enrollment, and ongoing clinical management.
  • Utilize critical thinking skills to assess and ensure the accuracy of study protocols and patient information.
  • Engage in administrative tasks and project management activities on non-clinic days to maintain efficient operations.
  • Collaborate with the Protocol Activation office to facilitate the initiation of new clinical trial protocols.
  • Review patient medical histories to verify eligibility for studies and gather necessary documentation.
  • Maintain proficiency in documenting and reporting serious adverse events and managing patient study calendars.

Qualifications:

  • Graduation from an accredited nursing program with a valid New Jersey nursing license.
  • Bachelor of Science in Nursing (BSN) is required.
  • A minimum of two years of nursing experience in a hospital setting, with at least one year in an oncology specialty.
  • Experience in a clinical research role is advantageous but not mandatory, as training will be provided.
  • Strong communication skills to effectively liaise with various departments and convey complex information to patients.
  • Proficiency in Microsoft Office applications and clinical trial management systems.
  • A proactive attitude and ability to thrive in a dynamic, academic environment.

Physical Requirements: Ability to stand, sit, walk, and lift up to 20 lbs. Regular communication and visual acuity are essential.

Important Note: Compliance with health requirements, including annual vaccinations, is mandatory for on-site roles.

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