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Cra Ii

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 Jobs Australia | ICON Careers

Meta Description

Apply for Clinical Research Associate II role at ICON in Australia. Remote work, clinical trial monitoring, ICH-GCP knowledge required. Join a leading biotech firm!

Meta Keywords

clinical research associate, CRA II jobs Australia, clinical trial monitoring, ICH-GCP jobs, remote clinical research, biotech careers Australia, pharmaceutical jobs Australia, clinical trial associate, ICON careers, healthcare jobs Australia


Clinical Research Associate II – Remote (Australia) | ICON

Job Summary

Join ICON plc, a world leader in healthcare intelligence and clinical research, as a Clinical Research Associate II (CRA II). This remote position offers an exciting opportunity to drive innovation in clinical trials across Australia. As a CRA II, you will ensure protocol compliance, data integrity, and patient safety in diverse clinical trials, supporting the advancement of new therapies. If you have a minimum of 2 years’ CRA experience, strong knowledge of ICH-GCP, and a passion for clinical development, this role is perfect for you.


Key Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials

  • Ensure strict adherence to protocol compliance and maintain high-quality clinical data

  • Collaborate effectively with investigators and clinical site staff to ensure smooth study conduct

  • Perform data reviews and resolve queries to maintain data accuracy and integrity

  • Assist in the preparation and review of essential clinical trial documentation, including protocols and study reports


Required Skills & Qualifications

  • Bachelor’s degree in scientific or healthcare-related field (e.g., Pharmacy, Life Sciences)

  • Minimum 2 years of experience as a Clinical Research Associate

  • Comprehensive knowledge of clinical trial processes, ICH-GCP guidelines, and regulatory requirements

  • Strong organizational, communication, and problem-solving skills

  • Ability to work independently and collaboratively in a remote, fast-paced environment


Perks & Benefits

  • Competitive salary (range not specified) with performance-based rewards

  • Various annual leave entitlements tailored to your location

  • Comprehensive health insurance options for you and your family

  • Competitive retirement planning to secure your financial future

  • Access to Global Employee Assistance Programme (LifeWorks) with 24/7 professional support

  • Life assurance coverage

  • Flexible, country-specific benefits including childcare vouchers, gym discounts, travel subsidies, and health assessments


About ICON plc

ICON plc is a leading global clinical research organization specializing in healthcare intelligence and biotech solutions. We are committed to innovation, inclusion, and excellence in clinical development, helping reduce the global disease burden by advancing cutting-edge therapies. ICON fosters a diverse, inclusive culture that empowers employees to thrive and contribute meaningfully to healthcare advancements worldwide.


Work Mode

Remote – Australia (Work from home with flexibility)


Call to Action

Ready to advance your clinical research career with a global leader? Apply now to become a Clinical Research Associate II at ICON and make a difference in healthcare innovation. Click Apply to submit your application today!