Oncology Research Registered Nurse (RN) – Norwalk, CT

Nuvance Health

Norwalk, CTFull-time

Behavioral Health Market Context

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Benefits

**$7,500 - Sign-On Bonus for Full-time externals only, pro-rated for Part-time****Exciting Opportunity for an Oncology Research Registered Nurse$ - $ Hourly

Qualifications

  • Bachelor's degree
  • Valid RN License (CT or NY based on Practice Location)
  • Basic Life Support (BLS)
  • Oncology nursing and chemotherapy/biotherapy administration
  • Knowledge of current standardized cancer reporting criteria; performance status, adverse event grading and tumor assessment
  • Registered Nurse
  • Bachelor's Level Degree
  • Some manual skills / motor coord & finger dexterity
  • Little or no potential for occupational risk
  • Sedentary/light effort
  • May exert up to 10 lbs. force
  • 8 more items(s)

Responsibilities

  • The Research Nurse will be committed to supporting the department's program's mission of conducting quality clinical research for our sponsors while providing safe and compassionate care to our patients
  • Works with physicians, the network oncology research director and other research staff and allied health professionals to coordinate clinical research efforts provided at Nuvance Health
  • Independently conducts procedures related to screening, eligibility, consent, registration, patient education, and data collection for cancer clinical trials
  • Prepares and submits to the IRB (Institutional Review Board) all required IRB documentation in a timely manner: including but not limited to new trial approval, sponsor submitted adverse events(SAE) information, annual updates, consent changes, and any patient SAE
  • Performs patient assessment and chemotherapy toxicity evaluation based on NCI CTCAE criteria for adverse events on treatment days and as needed
  • Collaborates with oncology physician practices and staff to assure protocol compliance and scheduling of patient visits
  • Tracks and enters clinical data on all cancer patients as required to include active patients and those in follow up in clinical trials
  • Participates in investigator and study initiation meetings
  • Assists with scheduling, reviewing clinical trial outline/content and preparing for monitor visits/audits with regulatory agencies or sponsors
  • Provides education to staff on cancer clinical trials through in-services, written materials and one to one interaction for each study, each patient and general marketing
  • Participates in oncology research meetings and multi-disciplinary case conferences
  • Identifies potential patients for clinical trial eligibility
  • Demonstrates flexibility in daily routine and effectively accommodates for the need of the job
  • Fulfills all compliance and regulatory responsibilities related to the position
  • Performs other duties as assigned
  • Generally pleasant working conditions
  • 13 more items(s)


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