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Clinical Research Associate Ii/ Senior Clinical Research Associate

2+ years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Full Time 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 - Melbourne & Sydney | ICON

Meta Description

Hiring Clinical Research Associate II / Senior CRA for oncology & global trials in Melbourne & Sydney. Remote role with ICON. 2+ years experience required.

Meta Keywords

clinical research associate jobs, senior clinical research associate Australia, CRA oncology jobs, clinical monitoring Melbourne, clinical trials Sydney, ICH-GCP clinical research, ICON clinical research jobs, remote CRA Australia


Clinical Research Associate II / Senior Clinical Research Associate

Location: Melbourne, Sydney (Home-based, Remote)
Employment Type: Full-Time
Work Mode: Remote (Home-based) with travel flexibility in Melbourne & Sydney


Job Summary

Join ICON, a global leader in clinical research and healthcare intelligence, as a Clinical Research Associate II / Senior CRA. This remote opportunity based in Melbourne or Sydney offers the chance to monitor global oncology and early development trials, ensuring data quality and regulatory compliance. Ideal for candidates with 2+ years of clinical monitoring experience, strong knowledge of ICH-GCP, and excellent communication skills. Expand your career in a company dedicated to innovation and patient-focused clinical development.


Responsibilities

  • Perform comprehensive CRA duties: site selection, initiation, routine monitoring visits, close-out, and database lock

  • Collaborate within client study teams and maintain strong communication with dedicated ICON line management

  • Oversee study site management ensuring high-quality clinical data with minimal queries

  • Ensure compliance with ICH-GCP, local regulations, and trial protocols

  • Provide mentoring and support to junior team members as needed

  • Travel as required within Melbourne, Sydney, and other locations


Required Skills & Qualifications

  • Degree in Pharmacy or a related field (B.Pharm, M.Pharm, or equivalent)

  • Minimum 2 years of prior monitoring experience with global clinical trials

  • Oncology monitoring experience is highly desirable

  • Strong understanding of international guidelines (ICH-GCP) and local regulations

  • Excellent verbal and written communication skills

  • Flexibility and willingness to travel as part of job requirements


Perks & Benefits

  • Competitive salary package (specific salary details not disclosed)

  • Remote work flexibility with supportive global clinical research infrastructure

  • Comprehensive health insurance plans tailored to employee needs

  • Generous annual leave entitlements

  • Retirement planning and life assurance options

  • Access to global Employee Assistance Program (TELUS Health) providing 24/7 wellbeing support

  • Flexible, country-specific benefits including childcare vouchers, gym discounts, and subsidized travel


Company Description

ICON plc is a world-leading clinical research organization specializing in biotechnology and pharmaceutical clinical trials. We provide data-driven, patient-focused solutions globally to accelerate medical innovation and improve health outcomes.


Work Mode

Remote (Home-based) with travel flexibility in Melbourne & Sydney


Call to Action

Ready to elevate your clinical research career? Apply now at ThePharmaDaily.com to join ICON’s cutting-edge clinical research team and contribute to innovative oncology and global trials.