Oncology Research Registered Nurse (RN) – Norwalk, CT
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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