Data Governance Tools to Advance Clinical Trial Data Sharing

About the Event

Are you a researcher or clinical trialist using secondary health data? Join us for an engaging and practical webinar jointly hosted by the CT:IQ at Bellberry Limited and ARDC, designed to help you navigate the complex secondary research landscape with clarity and confidence.

This session will introduce newly developed tools from CT:IQ and ARDC, created to support researchers working with secondary health data.

Through real-world case studies, we’ll highlight why good governance matters, and explore how these resources can help you better understand governance requirements, manage risk, and strengthen the integrity of your research.

If you work with secondary research health data, this webinar will provide practical insights, useful tools, and a clearer pathway through the governance landscape.

Speakers

• Dr Lisa Eckstein, Ethics Specialist and Director, CT:IQ at Bellberry
• Dr Marina Skiba, Clinical Trials and Governance Manager, Monash University Clinical Trials Centre
• Martijn Oostendorp, Associate Director, Clinical Trial Operations and Development, NHMRC Clinical Trials Centre

Who Should Attend

Secondary health data users, including:

• cinical trialists
• health and medical researchers
• data custodians and/or data managers
• human research ethics committee (HREC) members and professional staff

What You’ll Gain

• Understanding of the objectives of the Clinical Trial Data Governance Framework, and its focus on enabling responsible, transparent, and effective sharing of clinical research data in Australia
• Opportunity to explore the real-world implications of data governance decisions, particularly the impact on research participants, consumers, and public trust in medical research
• Discover the resources within the CT:IQ Resource Toolkit and learn how they can be practically applied to support compliant, ethical, and efficient secondary data use

Recording

This session will be recorded. The recording will be provided to all registrants and published on the ARDC YouTube channel.

Learn More

Learn more about the ARDC’s:

• Clinical Research Data Sharing Frameworks project and the resulting resource toolkit
• Health Data Australia service for finding and sharing health data
• Health Studies Australian National Data Asset (HeSANDA) program.

Do you have questions about this event? Contact us.

Please note that this event will be recorded and published by the ARDC. This may include your contributions during the session. Attendees are expected to comply with the Code of Conduct for ARDC Activities during this event. The ARDC respects the privacy of individuals. Information collected is in accordance with the ARDC Privacy Policy.

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