RN / Registered Nurse / New Jersey / Any / Oncology Clinical Research Nurses Job

3 weeks ago


Neptune, United States Odell Medical Search Full time

The Company:

  • Named one of Americas 250 Best Hospitals
  • Patient Safety Excellence Award

This company appreciates its employees:

  • Medical, Dental and Vision
  • Flexible Spending Account
  • Health Savings Account
  • PTO
  • 401k Savings Plans
  • Many other discounts and programs

The role you will play:

  • 40hrs Day Shift, 4-10s.
  • No weekends/no call/no holidays required.
  • Assures that all protocol revisions, informed consents, continuing reviews, serious adverse events are submitted to the appropriate IRB of record in a timely manner.
  • Interacts with regulatory specialists and principal investigators and sub-investigators on all regulatory issues and changes within the protocol.
  • In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
  • Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. Finalizes budget draft with budget coordinator.
  • Recruits and evaluates potential study patients and works with clinical research coordinator to schedule required appointments and interviews.
  • Identifies the needs of the patient population served and modifies and delivers care that is specific to those needs (i.e., age, culture, hearing and/or visually impaired, etc.)
  • This process includes communicating with the patient, parent, and/or primary caregiver(s) at their level (developmental/age, educational, literacy, etc.)

Background Profile:

  • Current and valid New Jersey Nursing license is required.
  • Must have Oncology Clinical Research experience.
  • Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC) is preferred.
  • Education on human subject research and GCP (CITI Training and Certification) is preferred.
  • Knowledge of clinical trials and the regulation (local, state, and federal) of such is preferred.
  • Familiarity with basic scientific and healthcare principles and terminology preferred.
  • BSN required.
  • Strongly prefer experience with medical oncology, solid tumors - GU, GI, Breast, Lung.


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