Skip to main content

About Us

Established & Proven

More than two decades of deep clinical research management experience

Avance Clinical is the largest specialist Australian and US CRO delivering quality clinical trials in Australia, New Zealand and North America for international biotechs.

The CRO has been delivering clinical drug development services for international biotechs for FDA and EMA regulatory approval, for more than two decades.


At Avance Clinical, our mission is to deliver world class clinical development today for your health tomorrow.

Our approach is designed to help biotechs bring innovative therapies to market in the most economically viable way, ensuring a successful and sustainable path to success. Please request a proposal today to discuss your next study or drug development program.

Early to Late Phase

Avance Clinical Australia and New Zealand teams focus on servicing biotech clients in their early phases of drug development delivering fast, nimble, and adaptive client-oriented solutions. In collaboration with our US operations, we also deliver later-phase CRO services.

Fast, nimble, and adaptive solutions

Avance Clinical delivers customized solutions designed around specific client needs rather than a one size fits all approach.

Clinical Monitoring Management

All Avance Clinical trials are monitored in accordance with Australian and New Zealand regulatory requirements and ICH GCP.

Learn More

ClinicReady - get into clinic faster

With ClinicReady, Avance Clinical’s team can act as a surrogate drug development department for start-up companies.

Learn More

Data Management

Avance Clinical data management team have gained a world-class reputation for accuracy, precision, and quality of their biostatistics and pharmacokinetic (PK) analysis.

Learn More


The Avance Clinical team works with eClinical leaders such as Medrio, Medidata and Oracle to offer regulatory compliant and patient-centric tools for rapid start-up and continual data flow.

Learn More

Project Management

Avance Clinical provides each clinical research trial with a dedicated Project Manager to ensure that milestones are reached, timelines are met and that our clients receive effective communication and ongoing status reports.

Learn More

Quality Assurance

Data quality is at the heart of everything at Avance Clinical. Delivered by our highly experienced staff we support our clients with their clinical trial audit to achieve their quality objectives for their clinical research trials.

Learn More

Safety and Pharmacovigilance

Clinical trials safety monitoring and reporting is vital to ensure participant safety, data integrity and regulatory compliance.

Learn More

Medical Writing

The Avance Clinical biostatistics and pharmacokinetics experts provide specialist guidance for your clinical research trial design and analysis.

Learn More

Full Service CRO

Avance Clinical is the leading full-service CRO for international biotechs conducting early Phase clinical trials.

The latest technology for data compliance

The company has focussed on state-of-the-art technology and systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, and Medrio are just some of the technology partners.

Avance Clinical offers globally accepted data from an established clinical trial ecosystem, that includes world-class PIs and Sites that are able to rapidly access specialized patient groups.

The Australian Government R&D grant means up to 43.5% rebate on clinical trial spend
Site Initiation Visit (SIV) and Study Start can be achieved in 5 – 6 weeks
Globally accepted data
No IND required for clinical trials

Request a Proposal or Talk to our Team  CONTACT US

More benefits

Avance Clinical can leverage all the benefits of Australia and New Zealand’s clinical ecosystem to deliver your study

Almost half clinical costs

The Government R&D grant means up to 43.5% rebate on clinical trial spend

Rapid Start-up

Site Initiation Visit (SIV) and Study Start can be achieved in 5 – 6 weeks

Start-up time

Site Initiation Visit (SIV) and Study Start can be achieved in 5 – 6 weeks


No IND required for clinical trials

GMP material

Full GMP material is not mandated for Phase I clinical trials

Gene-therapy accreditation

Avance Clinical is an accredited gene-therapy CRO

Seasonal studies

Northern hemisphere Sponsors can conduct their studies year-round by taking advantage of Australia and New Zealand's counter-flu and allergy seasons

FDA and global regulatory data compliance

Major hospitals with world-class infrastructures and dedicated Clinical Trial Units with a long track record in FDA compliant research


The Government R&D grant means up to 43.5% rebate on clinical trial spend

Start-up time

Site Initiation Visit (SIV) and Study Start achieved in 5 – 6 weeks


Full service CRO in Australia and New Zealand

An Experienced Team

Learn more about us here

Studies in the past 5 years
Experienced Team Members
Participants past 5 years
Years of of CRO experience

“Avance Clinical’s clients are international biotech companies primarily from the United States, United Kingdom, Japan, China, South Korea, Taiwan, France, and Germany. These clients are seeking a premium CRO with the same experience and advanced technology platforms offered by the major global CROs, but with an agile and customer focused approach to clinical management in Australia and New Zealand.”

Supriya Lala KunduBest Practices Research Analyst, Frost & Sullivan

Ready To Partner with Us?

Contact Us