Instagram
youtube
Facebook

Clinical Research Associate Ii/ Senior Clinical Research Associate

1-2 years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Meta Title:
Clinical Research Associate II – Remote, Brisbane

Meta Description:
Apply for Clinical Research Associate II/Senior CRA role in Brisbane. Work remotely in global vaccine trials. Competitive salary & growth opportunities.

Meta Keywords:
clinical research associate jobs Brisbane, CRA II jobs Australia, senior clinical research associate remote, ICON clinical trials, vaccine CRA jobs, remote CRA roles, clinical trials Australia, pharmaceutical research jobs


Job Title: Clinical Research Associate II / Senior CRA – Remote | Brisbane

Location: Remote (Brisbane, Australia)
Company: ICON plc
Job ID: 2025-119092
Employment Type: Full-Time
Salary Range: Not explicitly mentioned (competitive salary offered)


Job Summary

ICON plc, a world-leading healthcare intelligence and clinical research organization, is seeking an experienced Clinical Research Associate II or Senior CRA to support a global pharmaceutical partner in conducting vaccine studies. This is a home-based position in Brisbane, offering professionals the opportunity to work on innovative trials with a dedicated clinical operations team. Join ICON’s mission to advance the development of life-changing treatments through world-class research execution.


Key Responsibilities

  • Conduct on-site monitoring of vaccine clinical trials

  • Serve as the point-of-contact for study escalations with sites across NSW, VIC, and other Australian states

  • Maintain an up-to-date Clinical Trial Master File (CTMF)

  • Complete detailed and timely trip reports

  • Collaborate within a remote, cross-functional clinical team embedded with a single sponsor


Required Skills & Qualifications

  • Tertiary degree in a health, life sciences, or pharmacy discipline

  • Minimum 1–2 years of on-site monitoring experience (CRO or pharmaceutical environment preferred)

  • Strong understanding of ICH-GCP and local regulatory requirements

  • Excellent written and verbal communication skills

  • Full working rights in Australia

  • Ability to thrive in a fast-paced, remote setting


Perks & Benefits

  • Competitive salary (regionally benchmarked)

  • Various annual leave entitlements

  • Flexible, remote-first working arrangement

  • Comprehensive health insurance options for employees and families

  • Global Employee Assistance Program via TELUS Health

  • Life assurance and retirement planning

  • Optional wellness and lifestyle benefits (e.g., gym discounts, health assessments, childcare vouchers)


Company Overview

ICON plc is a global leader in clinical research and pharmaceutical development, committed to transforming healthcare through data-driven insights. With a presence in over 100 countries, ICON partners with top pharma, biotech, and medical device companies to deliver high-quality research that improves lives.


Work Mode: Remote (based in Brisbane, Australia)


Call to Action

Are you ready to advance your career in global vaccine research while working remotely? Join ICON and be part of a team reshaping the future of clinical development.
Apply today to start your journey with one of the most respected names in global clinical research.

Visit ICON Careers to learn more.