Life-changing science is our focus; we start there and everything else follows.

PYC Therapeutics is a clinical-stage biotech company discovering and developing RNA therapies designed to transform outcomes for patients living with rare genetic diseases.

We are entering a pivotal stage of growth as we advance our clinical programs, expand our pipeline, and continue building our position as a global RNA therapeutics company.

Our work spans inherited retinal disease, polycystic kidney disease, and neurodevelopmental disorders, alongside a broader discovery pipeline.

As our clinical portfolio continues to expand, we are seeking a Clinical Study Associate to support the operational delivery of clinical studies. Working closely with Clinical Study Managers and the Clinical Operations Manager, you will play an important role in coordinating study activities, maintaining essential documentation, supporting external partners and helping ensure studies are delivered to the highest standards of quality and compliance.

Your key responsibilities will include:

- Coordinate study activities, meetings, trackers, timelines and action items across assigned clinical studies
- Support the preparation, maintenance and management of study documentation and essential trial records
- Assist with the tracking of study progress, recruitment activities, site actions and operational deliverables
- Liaise with CROs, vendors, clinical trial sites and internal stakeholders to support effective study delivery
- Identify documentation gaps, quality issues and operational risks, escalating appropriately
- Support quality oversight activities and inspection readiness initiatives
- Prepare study updates, meeting minutes and operational reports

This is a full time opportunity, based in Sydney.





About You

You are an organised clinical research professional who enjoys coordinating complex study activities and working with CROs, vendors and clinical trial sites. Previous clinical site experience will be highly valued, particularly if you are looking to apply that insight in a sponsor-side role supporting high-quality trial delivery. You will also have demonstrated experience in the following:

- Minimum 3 years experience in clinical research, clinical trial coordination or clinical operations support.
- Understanding of ICH-GCP, clinical trial documentation requirements and applicable regulatory or ethics processes.
- Experience maintaining study files, trackers, action logs and clinical trial documentation.
- Strong organisational skills and attention to detail, with the ability to manage competing priorities.
- Clear and professional communication skills, with the confidence to liaise with internal stakeholders, CROs, vendors and clinical trial sites.
- Willingness to travel from time to time to support study, site or partner activities.

We are building a high-performance, science-led organisation where curiosity, collaboration, and pace matter.

Working at PYC provides the opportunity to:

- Contribute to clinical programs focused on rare genetic diseases with real patient impact.
- Build your clinical operations career within a growing clinical-stage biotechnology company.
- Work alongside experienced clinical development, quality and research professionals.
- Gain exposure across multiple clinical studies and global development activities.
- Access flexible working arrangements and additional leave benefits.

Closing Date: 7 August 2026 - PYC Therapeutics reserves the right to hire prior to the closing date.

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📌 Clinical Study Associate (New South Wales)
🏢 PYC Therapeutics
📍 New South Wales