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Clinical Trial Associate

2+ years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Hybrid 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 Trial Associate Job in Sydney | ICON Remote Hybrid

Meta Description

Apply for Clinical Trial Associate role in Sydney with ICON. Hybrid work, biotech & pharma experience preferred. Join leading global clinical research teams.

Meta Keywords

clinical trial associate Sydney, clinical research jobs Australia, biotech clinical trials Sydney, TMF management jobs, pharma clinical trial support, ICON careers Australia


Job Summary

Join ICON plc, a global leader in clinical research and biotechnology, as a Clinical Trial Associate based in Sydney with hybrid work options. This role offers a chance to support innovative pharmaceutical and biotech drug development programs focused on unmet medical needs. You will contribute to critical clinical trial operations including submission preparation, site coordination, and vendor management while working alongside top global pharma teams.


Responsibilities

  • Prepare and support regulatory submission packages (IRB/ERC and other regulatory bodies)

  • Manage trial and site administration including tracking and updating study metrics

  • Setup, maintain, and quality check Trial Master File (TMF/eTMF) documentation

  • Coordinate and liaise with clinical sites and internal/external stakeholders

  • Support drug supply planning, provision, destruction, and trial equipment management

  • Oversee coordination of vendors for printing, translation, and other outsourced services

  • Distribute site materials and clinical trial equipment

  • Organize meetings and communicate effectively across study teams


Required Skills & Qualifications

  • Prior clinical trial experience in pharmaceutical, biotechnology, or investigative site settings

  • Bachelor’s degree (BS/BA) or equivalent preferred

  • Working knowledge of Australian clinical trial startup processes

  • Detail-oriented, reliable, and passionate about clinical research

  • Basic understanding of Essential Documents, CFR, GCP, and ICH guidelines

  • Proficient in Microsoft Office, TMF systems, and Clinical Trial Management Systems (CTMS)


Perks & Benefits

  • Competitive salary (specific range not provided)

  • Hybrid work location based in Sydney, Australia

  • Various annual leave entitlements for work-life balance

  • Comprehensive health insurance options for employees and families

  • Competitive retirement planning and savings programs

  • 24/7 Global Employee Assistance Programme via TELUS Health

  • Life assurance coverage

  • Flexible benefits including childcare vouchers, bike purchase schemes, gym discounts, subsidised travel passes, and health assessments

More details at: https://careers.iconplc.com/benefits


Company Description

ICON plc is a global healthcare intelligence and clinical research organization specializing in pharmaceutical and biotechnology clinical trials. With a focus on innovation and unmet medical needs, ICON advances drug development programs worldwide to improve patient outcomes.


Work Mode

Hybrid – Sydney, Australia


Call to Action

Ready to make an impact in clinical research with a leading biotech company?
Apply now for the Clinical Trial Associate role at ICON and help shape the future of healthcare.