Clinical Research Nurse

2 months ago

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

Vitalief is seeking a highly skilled Clinical Research Nurse to join our team. As a key member of our clinical research team, you will be responsible for the implementation of Oncology Phase 1 related clinical trials at our Clinical Research Center (CRC) and ensuring that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and other applicable standard operating procedures and guidelines.

Key Responsibilities
  • Assist investigators to prepare and implement new clinical trials, screen and enroll study participants, and provide protocol-related clinical management to those participants while on study.
  • Ensure successful, patient-oriented, safe, and effective conduct of clinical trials.
  • Serve as a resource to other staff members on available protocols, and general research topics such as FDA, IRB, and GCP regulations.
  • Collaborate with the clinical research team to ensure timely prescreening of potential subjects and active cancer patients for all available clinical trials.
  • Review patient charts and medical history to confirm protocol eligibility and obtain source documents as needed.
  • Proactively manage, coordinate, and deliver high-quality, compassionate hands-on competent oncology nursing care and coordinate with the assigned clinical team, investigators, and ancillary departments as per protocol requirements and ensures adherence to the treatment plan and GCP guidelines.
  • Complete Serious/Unexpected Adverse Event (SAE) form for all internal and multicenter serious/unexpected adverse events as required by study sponsors, federal requirements, and institutional guidelines.
Requirements
  • Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.
  • Bachelor's Degree in Nursing preferred. Equivalent education, experience, and/or training may be substituted for the degree requirement.
  • Two or more years of nursing experience working in a hospital setting.
  • Minimum of 1 year or more years of experience working in an Oncology specialty area in a hospital or clinic setting.
  • Minimum of 6 months clinical research nursing experience.
  • Maintains active Basic Life Support (BLS) certification.
  • Must possess excellent communication and interpersonal skills to interact with subjects in a clear and confident manner.
  • Must be capable of independent decision-making, and multitasking.
  • Must be passionate in initiating, developing, and managing long-term relationships with patients and networks; encourage collaboration and input from all team members; and value the contributions of all team members.
  • Ability to gather relevant information systematically; break down problems into simple components; make sound decisions.
  • Passionate about approaching problems with curiosity and open-mindedness; offer new ideas, solutions, and/or options.
  • Proficient in computer applications (i.e., Oncore, Word, Excel, medical records database systems, etc.).
Physical Demands

Standing, sitting, walking, talking, and hearing. No special vision requirements. Lifting up to 25lbs.

Important Note

Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

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