Cancer Center in Northern, NJ area are seeking Oncology Clinical Research Nurses working with medical oncology, solid tumor patient population.

The Company:

• Named one of America’s 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 or someone who has a strong oncology nursing background and would be willing to be trained in clinical research.
• 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.