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Clinical Research Associate (Cra) – Remote | Icon Plc | Usa

Icon Plc
ICON PLC
1+ years
Not Disclosed
Remote, USA, Remote
1 May 7, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L.

Clinical Research Associate (CRA) – Remote | ICON plc | USA

Company: ICON plc
Job Title: Clinical Research Associate (CRA)
Location: United States (Remote)
Job Type: Full-Time
Work Mode: Remote
Job Requisition ID: JR150243


About ICON plc

ICON plc is a globally recognized clinical research organization (CRO) specializing in healthcare intelligence, clinical trial management, and drug development services. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of innovative therapies and improve patient outcomes worldwide.

ICON offers excellent career opportunities in clinical research, regulatory operations, pharmacovigilance, and clinical trial management across global markets.


Job Overview

ICON plc is hiring a Clinical Research Associate (CRA) to support the management and monitoring of clinical trials across multiple investigational sites in the United States.

The Clinical Research Associate will be responsible for:

  • Site monitoring visits
  • Clinical trial oversight
  • Data integrity verification
  • Patient safety compliance
  • Investigator site management
  • Regulatory documentation review

This is an excellent opportunity for clinical research professionals looking to grow their careers in remote clinical operations and site monitoring.


Experience Required

Minimum Experience

  • Minimum 9 months of onsite monitoring experience as a CRA

Experience Level

The final designation may vary based on total experience:

  • CRA I
  • CRA II
  • Senior CRA

Freshers Eligibility

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

Educational Qualification

Required Qualification

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 studies are conducted according to:
    • Protocol requirements
    • ICH-GCP guidelines
    • Regulatory standards

Site Management

  • Collaborate with:
    • Investigators
    • Clinical site staff
    • Sponsors
    • Internal study teams
  • Support smooth study execution and site compliance

Data Review & Quality Control

  • Review clinical trial data for:
    • Accuracy
    • Completeness
    • Data integrity
  • Resolve data queries and discrepancies

Documentation & Compliance

  • Assist with preparation and review of:
    • Clinical study reports
    • Trial protocols
    • Regulatory documents
    • Monitoring reports

Patient Safety

  • Ensure patient safety and ethical conduct throughout the clinical trial lifecycle