Built for Biotechs.

Services designed for lean teams scaling fast

Australian Market Entry

Australian
Market Entry

Your entry point to Australian clinical trials. I assess what you need, recommend the right delivery model, and build a strategy that balances speed, cost, and control.

Strategy
Regulatory & Submissions

Regulatory & Submissions

End-to-end regulatory support from HREC approvals to TGA pathways. I review protocols, handle drug importation, and compress approval timelines while maintaining full compliance.

Regulatory
Partner & Site Activation

Partner &
Site Activation

I activate trial sites and get them recruitment-ready. Leveraging established relationships across Australia, I streamline site agreements, accelerate approvals, and focus on what matters. Getting your participants to the clinic.

Operations
Owned-Site Development

Owned-Site
Development

Build independent clinical trial capability. From local council requirements to national regulations, I guide you through establishing your own site. Lower long-term costs, full operational control.

Capability
Trial Optimization

Trial
Optimization

Tailored trial delivery within your budget and timeline. From hands-on experience running owned operations, I help you cut inefficiencies, manage risk, and execute lean without compromising quality.

Efficiency
AI-Powered DocGen

AI-Powered
DocGen

Leverage AI tools and proven document strategies to accelerate your clinical submissions. From HREC packages to protocols, I get your documents to PI-review ready, reducing back-and-forth and freeing up your clinicians to focus on what they do best.

AI