Oncology Research Nursing Specialist

2 weeks ago

New Brunswick, New Jersey, United States Vitalief Full time
Why Choose Vitalief?

Vitalief stands at the forefront of healthcare consulting, dedicated to enhancing research efforts and revolutionizing clinical trials. We are currently in search of a skilled and passionate Oncology Clinical Research Nurse to become a vital part of our organization, committed to making a difference in the lives of patients through impactful research.

Benefits of Working with Us:
  • Contribute to groundbreaking scientific advancements that aim to improve patient outcomes.
  • Experience a culture that prioritizes personal and professional development.
  • Enjoy a healthy work-life balance with 20 PTO days and 9 paid holidays each year.
  • Receive comprehensive benefits including company-paid life insurance, short and long-term disability coverage, a 401K retirement plan, and various healthcare options.

Compensation:
Competitive salary based on experience.

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

Key Responsibilities:
  • Under the guidance of the Clinical Research Study Site Leader, support various Medical Oncology interventional studies, primarily focusing on solid tumors.
  • Deliver compassionate and competent oncology nursing care while collaborating with clinical teams, investigators, and ancillary departments to ensure compliance with protocols and Good Clinical Practice (GCP) guidelines.
  • Assist in the preparation and implementation of clinical trials, enrolling participants and managing their care throughout the study.
  • Demonstrate critical thinking and assertiveness in ensuring accurate protocol adherence and patient information management.
  • Engage in administrative tasks on non-clinic days, including documentation and project management activities.
  • Collaborate with the Protocol Activation office to initiate new clinical trial protocols.
  • Review patient records to confirm eligibility and obtain necessary documentation.
  • Record and report Serious Adverse Events (SAE) promptly and manage patient study calendars.

Qualifications:
  • Graduate from an accredited nursing program with a valid New Jersey nursing license.
  • Bachelor of Science in Nursing (BSN) required.
  • 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; training will be provided.
  • Strong communication skills to effectively convey complex information to patients.
  • Proficient in Microsoft Office applications and clinical trial management systems.

Physical Requirements:
Ability to perform tasks that involve standing, sitting, walking, and lifting up to 20 lbs.

Important Note:
Vitalief collaborates with major medical centers and academic institutions, necessitating annual influenza vaccinations and successful completion of a Mantoux Tuberculin Skin Test (TST) for tuberculosis.

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