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Clinical Trial Associate

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Onsite

Clinical Trial Associate

Hlx Life Sciences

Clinical Trial Associate

Skills

Google Cloud Platform

25 days ago

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Important information


Contract type:

Permanent

Location:

Australia

Work mode:

Onsite

Published on:

29 September 2026

What they need


Clinical Trial Assistant (CTA) – Australia

Location: Australia

Contract: Full-time, long-term contract

Therapeutic Area: Ophthalmology

Organisation: Specialist CRO

We are currently supporting a specialist CRO looking to appoint an experienced Clinical Trial Assistant (CTA) to support ongoing ophthalmology clinical trials across Australia.

This is a full-time, long-term contract opportunity, working closely with Clinical Project Managers, CRAs and wider study teams to provide operational and administrative support across the clinical trial lifecycle.

Key Responsibilities

  • Support the day-to-day operational delivery of ophthalmology clinical studies
  • Assist study teams across study start-up, maintenance and close-out
  • Maintain and quality-check TMF/eTMF documentation , ensuring completeness and inspection readiness
  • Collect, track and maintain essential study and regulatory documents
  • Maintain study trackers, timelines and clinical trial management systems
  • Support CRAs and Project Managers with site documentation and follow-up activities
  • Coordinate study meetings, documentation and study-related communications
  • Liaise with clinical sites and internal/external stakeholders
  • Support study metrics, reporting and trial documentation
  • Ensure activities are completed in accordance with ICH-GCP, SOPs and applicable Australian regulatory requirements

Requirements

  • Previous experience as a Clinical Trial Assistant, Clinical Trial Associate or similar Clinical Operations support role
  • Experience working within a CRO, biotechnology or pharmaceutical environment
  • Good understanding of ICH-GCP and clinical trial processes
  • Experience working with TMF/eTMF and clinical trial systems
  • Strong organisational skills and ability to manage multiple priorities
  • Excellent written and verbal communication skills
  • Ability to work effectively with CRAs, Project Managers and clinical sites
  • Previous ophthalmology experience is highly desirable , although strong CTA experience in other therapeutic areas will also be considered
  • Based in Australia with appropriate working rights

This is an excellent opportunity for a CTA looking for a stable, long-term contract within a specialist clinical research environment and the opportunity to gain further experience supporting ophthalmology studies.

If you’re interested in hearing more, please get in touch for a confidential discussion.

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