Clinical Research Nurse Specialist

1 week ago


Denver, Colorado, United States McKesson Full time
About Us

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization with a mission to advance therapies for patients worldwide. Focused on transforming care and personalizing treatment, SCRI has conducted over 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.

Our Team

We are proud to have a team of over 1,300 physicians actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S. Our research network brings together experts from various fields to deliver cutting-edge treatments and improve patient outcomes.

Job Description

We are seeking a highly skilled Clinical Research Nurse Specialist to join our team in the Colorado Blood Cancer Unit at Presbyterian St. Luke's Medical Center. As a key member of our team, you will be responsible for screening, enrolling, and following study subjects while ensuring protocol compliance and close monitoring.

You will review study design and inclusion/exclusion criteria with physicians and patients, verify informed consent procedures, and adhere to protocol requirements. Your primary responsibility will be to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.

As a Clinical Research Nurse Specialist, you will:

  • Enroll patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.
  • Review study design and inclusion/exclusion criteria with physicians and patients.
  • Verify informed consent procedures and adhere to protocol requirements.
  • Use the protocol as the only tool to screen, treat, and follow patients.
  • Complete and document screening/eligibility accurately.
  • Complete and document the informed consent process accurately and have all parties sign/date as required, including HIPAA Authorization.
  • Accurately complete and submit on-study forms within two weeks of enrollment.
  • Ensure that patient documentation is completed at each clinic visit while in screening.
  • Ensure that all medications are approved prior to initiating treatment or when changing medication regimens, such as crossover studies.
  • Accurately calculate and document BSA, Creatinine Clearance, Urine Protein: Creatinine ratio, and any other calculations or conversions required per protocol.
  • Ensure that follow-up appointments, scans, or related procedures are scheduled correctly according to protocol requirements.
  • Document appropriately when patients are removed from protocol.
  • Ensure reconsent of patients at the next scheduled visit, following availability of updated ICF, and documents process appropriately.
Requirements

To be successful in this role, you should have:

  • An Associate Degree; preferably a Bachelor's Degree.
  • RN License.
  • Knowledge of medical and research terminology.
  • Knowledge of FDA Code of Federal Regulations and GCP.
  • Knowledge of the clinical research processes.
  • At least one year of oncology experience, preferably hematology and/or transplant.
  • At least one year of experience in a research setting preferred.
  • Research Certification (ACRP or CCRP) Preferred.
Salary

The estimated salary for this position is $83,000 - $100,000 annually.



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