Cancer Center in Northern, NJ area is seeking an Oncology Phase I Clinical Research Nurse.
The Company
- Named one of Americas 250 Best Hospitals
- Received 2020 & 2021 Patient Safety Execellence 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 8:00 a.m. - 4:30 p.m. (5-8s)
- 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
- 3 years of clinical nursing experience or 1 year of clinical nursing experience with 2 years of clinical research experience is required
- 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 preferred