International Clinical Trial Collaborations Grant

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Grants of up to $3 million to support Australian-led participation in international clinical trials, generating evidence in usual care settings to improve healthcare outcomes nationally.

What is the International Clinical Trial Collaborations Grant Opportunity?

The MRFF 2026 International Clinical Trial Collaborations Grant Opportunity supports Australian-led participation in international clinical trials, with a focus on generating high-quality evidence to inform clinical care and improve patient outcomes.

Projects must involve a clinical trial conducted in Australia in collaboration with international partners, with recruitment not yet commenced at Australian sites.

This is a targeted and highly competitive funding round, designed for well-developed, trial-ready projects with strong international partnerships and clear pathways to translation.

International Clinical Trial Collaborations level of support

Funding Available

  • Total Funding Pool: $13,000,000
  • Grant Amount: Up to $3,000,000 per project
  • Minimum Grant Amount: Not specified
  • Grant Duration: Up to 7 years

Co-contribution

  • There is no co-contribution requirement specified; however, partner contributions (cash or in-kind) may strengthen an application.

International Clinical Trial Collaborations important dates

  • Minimum Data Due: 19 August 2026 (5:00pm ACT Local Time)
  • Application Close: 16 September 2026 (5:00pm ACT Local Time)
  • Register your interest with GrantHelper

International Clinical Trial Collaborations objectives

This program aims to:

  • Increase Australiaโ€™s involvement in global clinical trial networks
  • Support investigator-initiated international collaborative trials
  • Generate evidence in โ€˜usual careโ€™ settings to inform adoption into the Australian healthcare system

Projects and expenditure eligible for International Clinical Trial Collaborations support

Eligible projects must:

  • Involve investigator-initiated clinical trials conducted in Australia
  • Be delivered in collaboration with international research partners
  • Generate high-quality evidence on the effectiveness of:
    1. New or existing treatments
    2. Drugs
    3. Medical devices

  • Be conducted in โ€˜usual careโ€™ settings, supporting real-world clinical adoption
  • Demonstrate a clear pathway to improving health outcomes in Australia

Projects should address a defined health need and demonstrate strong potential for translation into clinical practice.

Funding will not support:

  • Pre-clinical studies
  • Phase I and Phase II clinical trials
  • Post-market monitoring studies
  • Research conducted primarily outside Australia
  • Indirect costs (e.g. organisational overheads, infrastructure, administration)
  • Funding for overseas trial sites (these must be funded by international partners)

Overseas expenditure is generally limited to 10% of total grant funding and must be clearly justified.

Other International Clinical Trial Collaborations important details that you will need to know

To be eligible, applicants must:

  • Be an approved MRFF Eligible Organisation (e.g. universities, medical research institutes, hospitals)
  • Submit applications via an eligible organisation (individual researchers cannot apply directly)
  • Nominate a Chief Investigator A (CIA) based in Australia
  • Ensure the project:
    1. Involves a clinical trial conducted in Australia
    2. Includes collaboration with international research partners
    3. Has not commenced recruitment at Australian trial sites

 

Joint (consortia) applications are encouraged, provided there is a lead eligible organisation.

Applications will be assessed against the following criteria:

1. Project Impact (40%)

  • Contribution to improved health outcomes, clinical practice, or policy
  • Alignment with MRFF objectives and Measures of Success
  • Strength of translation pathway into the Australian healthcare system
  • Evidence of meaningful consumer and stakeholder involvement

 

2. Project Methodology (30%)

  • Scientific quality and feasibility of the clinical trial design
  • Appropriateness of recruitment strategy, sample size, and trial methodology
  • Inclusion of robust governance, milestones, and performance indicators
  • Integration of consumer involvement and consideration of diversity (e.g. sex, gender)

 

3. Capacity, Capability and Resources (30%)

  • Strength and experience of the research team
  • Capability of international partners
  • Evidence of effective collaboration and established partnerships
  • Availability of resources and infrastructure to deliver the trial

 

4. Overall Value and Risk (Non-weighted)

  • Value for money and appropriateness of the budget
  • Strength of the risk management plan
  • Likelihood of delivering intended outcomes
  • Contribution to MRFF priorities

 

Applicants must:

  • Read and understand the guidelines.
  • Ensure eligibility for the funding. Applicants that do not meet all the eligibility criteria will not be considered.
  • Deliver the project as outlined in the application.
  • Provide complete information requirements.

 

Applicants should be prepared to provide:

  • A detailed clinical trial protocol and study design
  • Evidence of confirmed international partnerships and collaboration agreements
  • A Consumer Involvement Statement outlining engagement across all project stages
  • A Measures of Success Statement aligned with MRFF outcomes
  • A Risk Management Plan identifying and mitigating key project risks
  • Detailed budget justification across all expenditure categories
  • Letters of support from partner organisations (where applicable)
  • Evidence of funding for any overseas trial components

Applications must be submitted via NHMRCโ€™s online system, Sapphire.

Register your interestย with GrantHelperย to explore your alignment with this grant and how we can assist you to increase your chances of success.

International Clinical Trial Collaborations resources

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