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

Icon Plc
ICON PLC
2+ years
Not Disclosed
Detroit, Michigan, United States
1 May 7, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Labelling Assessment, MedDRA Coding, Medical Billing, 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 (CRA II) – Remote Clinical Research Job | ICON plc

Company: ICON plc
Job Title: Clinical Research Associate II (CRA II)
Location: Detroit, Michigan, United States
Job Type: Full-Time
Work Mode: Remote
Job Requisition ID: JR148678


About ICON plc

ICON plc is a leading global Clinical Research Organization (CRO) specializing in healthcare intelligence, clinical development, and innovative research solutions. The company partners with pharmaceutical, biotechnology, and healthcare organizations worldwide to accelerate drug development and improve patient outcomes through advanced clinical research services.

ICON offers exceptional career opportunities in clinical operations, monitoring, pharmacovigilance, regulatory affairs, and clinical data management.


Job Overview

ICON plc is hiring a Clinical Research Associate II (CRA II) for a remote clinical research role based in Detroit, Michigan.

As a CRA II, you will support and manage clinical trial monitoring activities while ensuring:

  • Protocol compliance
  • Data integrity
  • Patient safety
  • Regulatory adherence
  • High-quality clinical trial execution

This opportunity is ideal for experienced Clinical Research Associates looking to grow within a global CRO environment.


Experience Required

Mandatory Experience

  • Minimum 2 years of experience as a Clinical Research Associate (CRA)

Freshers Eligibility

  • Freshers are NOT eligible
  • Prior clinical trial monitoring experience is required

Educational Qualification

Required Degree

Bachelor’s degree in:

  • Life Sciences
  • Pharmacy
  • Nursing
  • Biotechnology
  • Healthcare
  • Related scientific discipline

Key Responsibilities

Clinical Trial Monitoring

  • Conduct:
    • Site Qualification Visits (SQV)
    • Site Initiation Visits (SIV)
    • Monitoring Visits (MV)
    • Close-Out Visits (COV)
  • Ensure clinical sites follow:
    • Study protocols
    • Regulatory guidelines
    • ICH-GCP standards

Site Management

  • Collaborate with:
    • Investigators
    • Site coordinators
    • Clinical staff
    • Sponsors
  • Support smooth clinical trial execution

Data Review & Compliance

  • Review clinical trial data for:
    • Accuracy
    • Completeness
    • Consistency
  • Resolve data queries and discrepancies promptly

Patient Safety Oversight

  • Monitor participant safety throughout study duration
  • Ensure ethical and regulatory compliance

Documentation Support

  • Assist in preparing and reviewing:
    • Clinical study reports
    • Monitoring reports
    • Protocol documentation
    • Regulatory records