As your dedicated Clinical Trial Partner, Complete Phase is purpose‑built for small to mid‑sized biotech and pharma innovators who demand a smarter, more agile approach to Phase 1 and Phase 2 clinical trials in Australia & New Zealand. With deep local expertise in clinical trial management Australia, we bring strategic insight, streamlined processes, and personal attention to every program.
Guiding principles
Your success is ours. We work with your team, not outside of it, collaborating side‑by‑side from protocol design through study close‑out. Proactive communication and shared goals keep timelines on track and budgets under control.
As your early‑phase specialist, we avoid the rigid templates of a big‑box provider and instead tailor every element to your science: site selection, patient recruitment, data capture, and more. Our nimble structure accelerates study start‑up and pivots quickly when needs evolve.
From first‑in‑human dose escalation to dose‑finding in oncology & CNS indications, our leadership averages 20+ years of hands‑on experience. We apply best practices in safety monitoring, biometrics, and regulatory compliance to safeguard participants, data integrity, and scientific rigor.
Our Clinical Operation experts design and manage every phase 1 and 2 trial element, from protocol development and site selection to patient recruitment and logistics, ensuring streamlined execution and on‑time milestones.
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Our Regulatory Affairs navigators chart an efficient path for your investigational product’s success, managing submissions, approvals, and communications with Australia’s TGA and HREC (our version of an IRB!) to accelerate trial initiation.
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Our specialists deliver clinical oversight throughout the trial lifecycle, guiding protocol development, meticulously conducting safety assessments, managing adverse event reporting, and partnering with investigators to safeguard participant well‑being.
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All clinical trials in Australia require a local sponsor. Complete Phase can act as your local sponsor, handling TGA CTN submission and medico‑legal duties while also helping you establish a subsidiary with a Resident Director and expert R&D tax support.
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Our Pharmacovigilance team implements comprehensive drug safety monitoring from adverse event collection and signal detection to risk management, safeguarding participant welfare and regulatory compliance.
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Our Biometrics services deliver robust biostatistics support: statistical planning, data analysis, and reporting that transform raw trial data into actionable insights for confident decision‑making.
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With over 50 years of collective experience, our leadership has kept us at the forefront of complex Oncology, Immunology, and CNS clinical trials in Australia. We combine deep scientific insight with agile execution to accelerate your therapeutic development from first-in-human through proof-of-concept.
With us as your Clinical Trial Partner, we take you on an efficient, painless, and scientifically rich journey through end‑to‑end early phase trial services. Reach out to explore how Complete Phase can accelerate your next milestone.
See how we operate