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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 – Remote Melbourne Sydney

Meta Description

Hiring Clinical Research Associate II/Senior CRA for global biotech trials in Melbourne & Sydney. Remote role with ICON. Apply now for oncology & early development jobs.

Meta Keywords

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


Job Summary

Join ICON plc, the world’s largest clinical research organization powered by healthcare intelligence, as a Clinical Research Associate II / Senior Clinical Research Associate based remotely in Melbourne or Sydney. Work alongside a leading global biotechnology company focused on innovative oncology and hematology trials, early development studies, and diverse therapeutic areas. This opportunity offers dynamic involvement in global clinical trials with comprehensive support and career growth.


Responsibilities

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

  • Manage study sites ensuring data quality with low query levels and compliance to regulatory standards

  • Collaborate closely with the client’s study team, embedded in the study with dedicated ICON line management support

  • Maintain documentation and reporting to meet quality assurance requirements

  • Support adherence to ICH-GCP and local regulatory guidelines

  • Travel as required to support site visits and monitoring activities


Required Skills & Qualifications

  • Degree in Pharmacy or related life sciences field

  • Minimum 2+ years monitoring experience in global clinical trials, preferably with oncology exposure

  • Strong knowledge of international guidelines including ICH-GCP and local regulatory requirements

  • Excellent communication and interpersonal skills

  • Flexibility to travel within Australia

  • Full working rights in Australia


Perks & Benefits

  • Competitive salary (not explicitly stated) and performance rewards

  • Remote work flexibility with a supportive global team

  • Various annual leave entitlements

  • Comprehensive health insurance plans suitable for employees and families

  • Competitive retirement savings and planning programs

  • Access to 24/7 Employee Assistance Programme (TELUS Health)

  • Life assurance coverage

  • Additional benefits such as childcare vouchers, bike purchase schemes, gym discounts, subsidised travel passes, and health assessments

For full details, visit ICON careers: https://careers.iconplc.com/benefits


Company Description

ICON plc is a leading global healthcare intelligence and clinical research organization specializing in pharmaceutical, biotechnology, and medical device clinical trials. ICON drives innovation across multiple therapeutic areas with a commitment to improving patient outcomes worldwide.


Work Mode

Remote (Home-based) – Candidates should be located in or near Melbourne or Sydney, Australia.


Call to Action

Ready to advance your career in clinical research with a global biotech leader?
Apply now to join ICON’s team and contribute to cutting-edge oncology and early development clinical trials.