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Clinical Research Associate Ii (Oncology) – Remote Cra Job In Chicago | Icon Plc

Icon Plc
ICON PLC
2+ years
$91,336 – $114,170 per year
Chicago, Illinois, USA, United States
2 May 7, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Associate II (Oncology) – Remote CRA Job in Chicago | ICON plc

Company: ICON plc
Job Title: Clinical Research Associate II – Oncology
Location: Chicago, Illinois, United States
Work Mode: Remote
Job Type: Full-Time
Job Requisition ID: JR149492
Salary Range: $91,336 – $114,170 per year


About ICON plc

ICON plc is a globally recognized Clinical Research Organization (CRO) delivering advanced healthcare intelligence, clinical development, and pharmaceutical research services worldwide. The company partners with biotech, pharmaceutical, and healthcare organizations to accelerate innovative drug development and improve patient outcomes through high-quality clinical research solutions.

ICON offers excellent career opportunities across:

  • Clinical Operations
  • Oncology Research
  • Pharmacovigilance
  • Regulatory Affairs
  • Clinical Data Management
  • Medical Monitoring

Job Overview

ICON plc is hiring a Clinical Research Associate II (CRA II) – Oncology for a remote clinical monitoring role based in Chicago, Illinois.

The selected candidate will manage oncology clinical trial monitoring activities, ensure protocol compliance, oversee patient safety, and maintain high-quality clinical data throughout the study lifecycle.

This role is ideal for experienced oncology CRAs seeking career growth in a global CRO environment.


Experience Required

Mandatory Experience

  • Minimum 2+ years of on-site monitoring experience in:
    • Pharmaceutical industry
    • CRO industry
  • Prior experience monitoring Oncology clinical trials is mandatory
  • Hematology/Oncology (Heme/Onc) monitoring experience preferred

Freshers Eligibility

  • Freshers are NOT eligible
  • Prior CRA monitoring experience is required

Educational Qualification

Required Degree

  • Bachelor’s degree in:
    • Life Sciences
    • Pharmacy
    • Biotechnology
    • Healthcare
    • Related scientific discipline

OR

  • Qualified Registered Nurse (RN)

Key Responsibilities

Clinical Trial Monitoring

  • Conduct:
    • Site Selection Visits
    • Site Initiation Visits
    • Routine Monitoring Visits
    • Site Close-Out Visits
  • Ensure study sites comply with:
    • ICH-GCP guidelines
    • SOPs
    • Regulatory requirements

Site & Sponsor Coordination

  • Serve as the primary contact between:
    • Investigational sites
    • Sponsors
    • Clinical teams

Patient Safety Oversight

  • Monitor:
    • Adverse Events (AE)
    • Serious Adverse Events (SAE)
    • Product Quality Complaints (PQC)
  • Ensure timely reporting and compliance

Clinical Systems Management

  • Maintain accurate records in:
    • CTMS
    • eTMF systems
  • Track site staff training and compliance documentation

Data Quality Management

  • Resolve clinical data queries
  • Ensure accurate and timely data entry
  • Monitor study progress and escalate risks when required

Drug Accountability

  • Oversee investigational product:
    • Storage
    • Accountability
    • Return/destruction procedures

Cross-Functional Collaboration

  • Work closely with:
    • CTAs
    • LTMs
    • CTMs
    • Clinical Operations Teams