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Sarah Cannon Research Institute

Community-based oncology clinical research organization

Infusion Research Nurse - PRN

Nursing & Frontline Patient CareConfirmed live in the last 24 hours
Part-timeDenver, CO, USA$40 - $52 /hr

About the Job

Requirements

  • An Associate Degree; preferably a Bachelor’s Degree
  • Current licensure in the state of Colorado as a Registered Nurse
  • Knowledge of medical and research terminology
  • Knowledge of FDA Code of Federal Regulations and GCP
  • Knowledge of the clinical research processes
  • Knowledge of Phase I protocol preferred
  • One year of acute care nursing experience required
  • At least on year of oncology experience preferred
  • At least one year of experience in a research setting preferred
  • Current BLS certification
  • Current ACLS certification (can complete within 30 days of start date)
  • ONS Chemotherapy Provider card
  • Research Certification (ACRP or CCRP) Preferred

Responsibilities

  • You will closely follow study patient(s) throughout treatment course ensuring protocol compliance
  • You will administer chemotherapy as ordered by physicians
  • You will read and interpret EKGs
  • Must communicate all protocol related issues/problems to the investigator
  • You will assess patient for side effects of treatment and symptoms related to disease or disease progression
  • You will assess lab data and communicates abnormal findings to the investigator and oncologist
  • You will assess and document patient compliance with medications and return visits
  • You will communicate with the pharmacy staff to provide timely and accurate study drug distribution
  • You will maintain a current medication list and records in protocol specific requirements
  • You will provide data team with completed follow-up forms, medical records, lab data and other source documents in a timely manner
  • You will educate and orient ancillary staff in study specific procedures
  • You will document and report adverse events
  • You will perform telephone triage
  • Assesses the patients EMR to ensure that all required data has been entered prior to patients scheduled appointment
  • You will perform patient counseling and referral to appropriate support services
  • You will monitor schedules daily for appropriate treatment distribution and additional patient visits

Desired Qualifications

  • Knowledge of Phase I protocol preferred
  • One year of oncology experience preferred
  • At least one year of experience in a research setting preferred
  • Research Certification (ACRP or CCRP) Preferred

About the Company

Sarah Cannon Research Institute

Community-based oncology clinical research organization

Sarah Cannon Research Institute (SCRI) is a global oncology research organization that conducts cancer clinical trials in community settings, partnering with pharmaceutical and biotech sponsors, physicians, and patients to develop new treatments. It works as an oncology-focused contract research organization (CRO) and centralized site management organization (SMO), running trials across more than 200 locations with roughly 1,500 research physicians, and applies technology such as its Accelero platform to personalized-medicine studies. Over more than 30 years it has completed more than 900 first-in-human trials across early- to late-phase research. What sets SCRI apart is this community-based model paired with early-phase depth, which has helped advance most new cancer therapies the FDA approved in the past decade. The goal is to accelerate oncology research from early trials to approval and bring advanced cancer treatments to patients.

Company size
1-10
Company stage
Not listed
Total funding
Not listed
Headquarters
Beach Haven, NJ
Founded
Not listed

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