RN / Registered Nurse / New Jersey / Any / Oncology Clinical Research Nurses Job - Neptune, United States - Odell Medical Search

    Odell Medical Search
    Odell Medical Search Neptune, United States

    1 month ago

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    Description

    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.