At Complete Phase, we tailor our clinical operations management to the unique needs of each medical innovation. As your trusted clinical trial partner, we integrate end‑to‑end solutions and streamline trial execution and oversight so you can focus on the science.
We understand that our out-of-country clients seeking successful Phase 1 and Phase 2 clinical trials in Australia & New Zealand need more than a hands-off checklist approach. Our flexible clinical trial management model adapts to your timelines and budget, leveraging site selection & feasibility expertise, patient recruitment optimization, and real‑time operations oversight to keep your program on track.
Together with in‑house experts and renowned Key Opinion Leaders (KOLs), we provide clinical trial strategic consulting to inform go‑to‑clinic roadmaps, feasibility and gap analyses, and risk‑mitigation planning. Your study benefits from data‑driven trial strategy and portfolio prioritization guidance that maximizes your product’s potential from the outset.
Our clinical trial project management framework ensures end‑to‑end coordination of every milestone, deliverable, and resource. A dedicated Project Manager will oversee budget and timelines, align cross‑functional teams, and deliver transparent governance—so you gain confidence that your trial will be conducted on time, within budget, and to the highest standards.
We combine risk‑based monitoring and source data verification to safeguard participant safety and data integrity. Our Clinical Research Associates (CRAs) combine high-caliber qualifications with excellent interpersonal skills to build and maintain effective relationships with the site staff throughout the life cycle of the study. Benefit from adaptive plans, comprehensive site performance reviews, and real‑time issue flagging to proactively address challenges and maintain regulatory compliance.
From electronic Trial Doc setup to HREC submission packages and SOP development, our trial documentation team keeps you audit‑ready at every step. We manage regulatory dossiers, version control, and quality‑control document review to ensure your submission to TGA and ethics committees proceeds smoothly and on schedule.
Our data management services harness agile eCRF platforms and streamlined workflows to capture high‑quality data. Paired with biometrics expertise—statistical planning, programming, and analysis—we translate raw trial data into actionable insights that support go/no‑go decisions and regulatory submissions.
As a niche collaborator with over 50 years of collective experience, our leadership has kept us at the forefront of complex Oncology 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. We don’t just work for you, we work with you: our customized, agile support, proactive communication, strategic foresight, and veteran leadership ensures your every trial meets stringent standards for safety, compliance, and scientific rigor.
Ready to elevate your early‑phase clinical operations? Contact your dedicated clinical trial partner today to learn how Complete Phase can accelerate your next milestone.