Clinical Research Nurse

The Clinical Research Nurse (CRN) manages clinical trials for patients with lymphoma. This role coordinates trial protocols, ensures patient safety, and collects high-quality data. The CRN acts as a vital bridge between lymphoma patients, oncology physicians, and clinical trial sponsors.

Key

• Patient Management
  :
  Screen, recruit, enroll, and educate patients on lymphoma clinical trials.
• Trial Coordination
  :
  Schedule research visits, diagnostic tests, and protocol-specific laboratory testing.
• Clinical Care
  :
  Administer investigational products and monitor patients for adverse events (AEs).
• Data Integrity
  :
  Document research data accurately in Electronic Data Capture (EDC) systems.
• Regulatory Compliance
  :
  Maintain regulatory binders and adhere to FDA, ICH-GCP, and Institutional Review Board (IRB) guidelines.
• Collaboration
  :
  Partner with principal investigators, pharmaceutical sponsors, and the hematology-oncology care team.

• Education
  :
  Graduate of an accredited school of nursing.
• Licensure
  :
  Active Registered Nurse (RN) license in the state of practice.
• Certifications
  : BLS certification required.
• Skills
  :
  Proficient with Electronic Health Records (EHR) and data management systems.

• Education
  :
  Bachelor of Science in Nursing (BSN).
• Experience
  :
  Minimum 2 years of oncology, hematology, or clinical research nursing experience.
• Certifications
  :
  Certified Clinical Research Coordinator (CCRC) or Oncology Certified Nurse (OCN) designation.