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Clinical Trial Associate

1-2 years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Full Time 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 Sydney | ICON Careers

Meta Description

Hiring Clinical Trial Associate in Sydney (Hybrid). Join ICON biotech, support clinical trials, and ensure compliance with GCP/ICH standards. Apply now!

Meta Keywords

clinical trial associate jobs Sydney, clinical trial support Sydney, biotech jobs Australia, TMF management, clinical research Sydney, ICON clinical trials, GCP clinical trial jobs, pharmaceutical clinical trial associate


Clinical Trial Associate – Sydney (Hybrid)

Location: Sydney, Australia (Hybrid Work Model)
Employment Type: Full-Time


Job Summary

Join ICON, a leading global biotechnology and pharmaceutical company, as a Clinical Trial Associate based in Sydney. In this hybrid role, you will support clinical trial operations, ensure accurate study documentation, and collaborate with clinical sites and stakeholders. This is a fantastic opportunity for candidates with clinical trial experience and knowledge of GCP/ICH guidelines to grow within a global organization committed to advancing healthcare innovation.


Responsibilities

  • Prepare submission packages for IRB/ERC and regulatory agencies

  • Track and update clinical trial metrics and site administration tasks

  • Set up and maintain Trial Master File (TMF) and electronic TMF (eTMF), ensuring document quality and completeness

  • Liaise with clinical trial sites, internal teams, and external stakeholders to coordinate trial activities

  • Manage drug supply planning, provision, destruction processes, and trial equipment logistics

  • Coordinate vendor activities including printing, translation, and material management

  • Distribute site materials and organize meetings related to trial operations


Required Skills & Qualifications

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

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

  • Working knowledge of Australian study start-up processes and regulatory requirements

  • Familiarity with Essential Documents, CFR, and GCP/ICH guidelines

  • Proficiency with Microsoft Office, TMF systems, and Clinical Trial Management Systems (CTMS)

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


Perks & Benefits

  • Competitive salary (specific range not disclosed)

  • Flexible hybrid work arrangement in Sydney

  • Annual leave entitlements aligned with Australian standards

  • Comprehensive health insurance options for employees and their families

  • Retirement planning and life assurance programs

  • Access to the Global Employee Assistance Programme (TELUS Health) offering 24/7 wellbeing support

  • Flexible country-specific benefits such as childcare vouchers, gym discounts, subsidized travel, and health assessments


Company Description

ICON plc is a globally recognized clinical research organization delivering innovative solutions for pharmaceutical and biotech companies. With a strong focus on advancing healthcare through clinical trial excellence, ICON fosters a culture of diversity, inclusion, and high performance.


Work Mode

Hybrid (Sydney-based with a mix of remote and onsite work)


Call to Action

Ready to make an impact in clinical research? Apply now at ThePharmaDaily.com to join ICON as a Clinical Trial Associate and contribute to cutting-edge biotechnology trials in Sydney.