Oncology Clinical Research Specialist

1 week ago

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

Why Choose Vitalief?
Vitalief is a pioneering healthcare consulting firm dedicated to enhancing research capabilities and transforming clinical trials. We are in search of a passionate and skilled Oncology Clinical Research Nurse to become a vital part of our remarkable team. This role offers a unique opportunity for nurses with oncology experience to transition into a fulfilling career within the clinical research field.

Benefits of Joining Vitalief:

  • Play a key role in our clients' mission to advance scientific breakthroughs that can significantly improve patient outcomes.
  • Experience a PEOPLE FIRST culture that emphasizes both personal and professional development for all employees.
  • Contribute to an environment that fosters innovation and values every team member's input.
  • 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 a variety of healthcare options.

Compensation: Competitive salary based on experience level.

Work Environment: This position requires on-site work five days a week, with the option to work remotely one day per week after a training period.

Key Responsibilities:

  • Under the guidance of the Clinical Research Study Site Leader, support various Medical Oncology interventional studies (phases I to III) focusing on Solid Tumor, Lung, Head and Neck, Melanoma, and Neurology.
  • Deliver high-quality, compassionate oncology nursing care while coordinating with the clinical team, investigators, and ancillary departments to ensure compliance with treatment protocols and Good Clinical Practice (GCP) standards.
  • Assist physicians in preparing and implementing new clinical trials, screening and enrolling participants, and providing protocol-related clinical management.
  • Utilize critical thinking skills to prioritize tasks and ensure accuracy in patient information relative to study protocols.
  • Manage patient interactions on designated clinic days while performing administrative duties on non-clinic days, including documentation and project management activities.
  • Collaborate with the Protocol Activation office to initiate and activate new clinical trial protocols using the Oncore Study-start up task list.
  • Review patient charts and medical histories to confirm eligibility for protocols and obtain necessary source documents.
  • Demonstrate proficiency in core tasks such as recording Serious Adverse Events (SAE), accessing protocol attachments, and managing patient study calendars.

Qualifications:

  • Graduation from an accredited nursing program with a valid nursing license in New Jersey.
  • Bachelor of Science in Nursing (BSN) degree.
  • A minimum of 2 years of nursing experience in a hospital environment.
  • At least 1 year of experience in an Oncology specialty area within a hospital or clinic.
  • Experience in a clinical research role is advantageous but not mandatory; training will be provided.
  • Strong critical thinking skills and the ability to communicate effectively with other departments and patients.
  • Proficiency in document management and familiarity with Microsoft Office applications.
  • Detail-oriented with the ability to thrive in a dynamic, academic, and diverse environment.
  • Proactive approach to learning and problem-solving.

Physical Requirements: The role involves standing, sitting, walking, visual perception, and communication. Ability to lift up to 20 lbs is required.

Important Note: Vitalief collaborates with major medical centers and academic institutions, which may require all on-site personnel to meet specific health requirements.

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