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Clinical Trial Assistant

C01 Cochlear Limited · The Rocks, Sydney

How to use this kit

Ground every answer in facts on this page and the original listing. We never invent Glassdoor-style reviews or salaries that are not in our data.

Interview prep

Expect scenarios on document control, prioritizing conflicting deadlines, and communicating protocol changes. Prepare a brief example of tracking detail under pressure and questions about the trial portfolio and team structure at this Sydney site.

Fit summary

Best for organized communicators who like process accuracy more than direct patient care. On-site in The Rocks (not remote); comfort with regulated paperwork and collaborative trial teams matters more than a clinical title alone.

Day in the role

As a Clinical Trial Assistant at Cochlear Limited in The Rocks, a typical day supports trial operations: filing and tracking essential documents, scheduling visits, preparing site packs, logging queries, and liaising with coordinators, monitors, and vendors so study activities stay audit-ready and on timeline.

Skills to emphasize

Build trial-admin fluency (eTMF basics, ALCOA, visit logistics) plus clear written updates. Free learning options:

FAQ from this listing

Is this role remote?

No. The listing is on-site in The Rocks, Sydney.

What does a Clinical Trial Assistant mainly do?

Supports study operations—documentation, scheduling, packing, and query follow-up—so trials stay compliant and coordinated.

Are free upskilling options listed?

Yes: Saylor Health Sciences courses (free) and Coursera audit-track healthcare courses (free to learn).

Role overview (listing rewrite)

Clinical Trial Assistant at C01 Cochlear Limited - The Rocks, Sydney Role Overview The position of Clinical Trial Assistant at C01 Cochlear Limited is a full-time role based in The Rocks, Sydney. This opportunity requires immediate attention as the company reserves the right to close this advertisement at any time. Your Responsibilities Assist with the coordination and management of clinical trials for implantable hearing solutions Support data collection, documentation, and reporting in compliance with regulatory requirements Ensure accurate and timely communication between various stakeholders involved in the clinical trial process Contribute to the preparation of study protocols, case report forms, and other relevant documents Maintain a high level of confidentiality regarding sensitive patient data What We're Looking For A degree in healthcare-related field or equivalent experience Familiarity with clinical trial processes and regulations <liStrong organizational, communication, and attention to detail skills Experience in data management is a plus Proficiency in Microsoft Office Suite and other relevant software applications Why Join C01 Cochlear Limited Cochlear's mission is to help people hear and be heard. As the global leader in implantable hearing solutions, we are dedicated to transforming the way people understand and treat hearing loss. Our team of professionals works towards creating a world full of sound for individuals with moderate to profound hearing loss. Next Steps To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. Please submit your application as soon as possible due to the company's right to close the advertisement at any time.

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Questions to ask them

Generated for personal interview prep · 2026-08-13 UTC · getajob.ai