ActalentVerified Source

Clinical Research Nurse Coordinator, Oncology & OnCore Experience

114K–125K
Onsite · New York, New York
Posted August 14, 2026
full-time

Overview

Own the coordination and execution of oncology clinical trials from screening to follow-up for a major research program. You will operate onsite in New Brunswick, collaborating with investigators, oncology teams, and supporting staff to ensure protocol adherence and patient safety. This role offers exposure to regulatory compliance, GCP, IRB processes, and sponsor communications within a contract-to-hire pathway.

What You'll Do10

  • 1Build patient screening and enrollment processes for oncology trials to meet protocol timelines
  • 2Design and conduct informed consent discussions in accordance with GCP and IRB requirements, documenting the process
  • 3Lead coordination of protocol-required visits, treatments, labs, imaging, and follow-up care to ensure participant safety
  • 4Own adverse event monitoring and SAEs reporting with accurate source documentation and regulatory compliance
  • 5Collaborate with multidisciplinary teams to maintain protocol compliance and data integrity across sites
  • 6Drive case report form completion and clinical trial database management to support data quality
  • 7Ship study materials, coordinate start-up activities, monitoring visits, audits, and sponsor communications
  • 8Scale patient education and ongoing communication to improve participant retention and engagement
  • 9Audit and maintain study records and regulatory files to ensure FDA, IRB, and institutional compliance
  • 10Support research operations from start-up to close-out, enabling smooth project delivery

Requirements7

  • 1Bachelor of Science in Nursing (BSN) with active New Jersey RN license
  • 2Experience reviewing medical records and identifying eligible patients for clinical trials
  • 3Experience with informed consent, adverse event reporting, and protocol management
  • 4Familiarity with OnCore, EDC systems, EMRs, and clinical trial documentation
  • 5Knowledge of FDA regulations, IRB requirements, and Good Clinical Practice (GCP)
  • 6BLS certification and chemotherapy certification
  • 7OCN, AOCN, CCRP, CRA, or other research-related certifications preferred

Salary Insight

$114 - $125k per year

Location

Typeonsite
LocationNew York, New York

Required Skills

OnCoreEDC systemsEMRsFDA regulationsIRB requirementsGood Clinical PracticeBLS certificationChemotherapy certificationOCNAOCNCCRPCRAInformed consentAdverse event reportingProtocol management
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