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

Icon Plc
ICON PLC
2+ years
Not Disclosed
California, 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: 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: Long Beach, California, United States
Work Mode: Remote
Job Type: Full-Time
Job Requisition ID: JR147421


About ICON plc

ICON plc is a globally recognized Clinical Research Organization (CRO) providing healthcare intelligence, clinical development, and innovative research solutions to pharmaceutical, biotechnology, and healthcare companies worldwide.

The organization supports groundbreaking clinical trials and offers career opportunities across clinical operations, monitoring, pharmacovigilance, regulatory affairs, and clinical data management.


Job Overview

ICON plc is seeking an experienced Clinical Research Associate II (CRA II) to support remote clinical trial monitoring activities in the United States.

As a CRA II, you will be responsible for:

  • Monitoring clinical trial sites
  • Ensuring patient safety
  • Maintaining protocol compliance
  • Supporting regulatory adherence
  • Managing clinical trial documentation and site activities

This role is ideal for professionals with prior CRA experience who want to work in a dynamic global clinical research 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 mandatory

Educational Qualification

Required Degree

Bachelor’s degree in:

  • Life Sciences
  • Pharmacy
  • Biotechnology
  • Nursing
  • 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 compliance with:
    • Study protocols
    • ICH-GCP guidelines
    • Regulatory standards

Patient Safety & Compliance

  • Ensure participant safety throughout study execution
  • Maintain data integrity and regulatory compliance

Site Management

  • Collaborate with:
    • Investigators
    • Site coordinators
    • Clinical staff
    • Sponsors
  • Support efficient trial operations and issue resolution

Clinical Data Review

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

Study Documentation

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

Required Skills

Clinical Research Skills

  • Clinical Trial Monitoring
  • Site Management
  • Clinical Operations
  • Patient Safety Oversight
  • Regulatory Compliance
  • ICH-GCP Knowledge
  • Clinical Documentation

Technical Skills

  • EDC Systems
  • CTMS Platforms
  • Clinical Trial Software
  • Data Review Tools

Soft Skills

  • Communication Skills
  • Problem Solving
  • Time Management
  • Organizational Skills
  • Attention to Detail
  • Team Collaboration