Unlock the potential of secondary data from clinical trials with HDA

Join us for a webinar exploring secondary data usage within clinical trials using Health Data Australia.

Health Data Australia is a national catalogue of Australian health data for researchers to discover and request access to data for their research. Over 72 health research organisations from across Australia contribute to Health Data Australia. The establishment of this network of providers was part of the ARDC-coordinated Health Studies Australian National Data Asset (HeSANDA) initiative, which began in 2021 and continues under the ARDC People Research Data Commons.

Hear from expert clinical researchers who use secondary data from trials to increase and improve their research. Learn about the 4 key domains for data reuse and hear about case studies highlighting the potential benefits and considerations when using secondary data in your research.

This webinar will guide you to uncover strategies to optimise your approach to using secondary clinical trial data and maximise the impact of your work.

Who will be speaking?

• Dr Anna Lene Seidler PhD, MSc, BSc Senior Research Fellow, Team Lead, NextGen Evidence Synthesis, Research Associate, Australian New Zealand Clinical Trials Registry (ANZCTR), and Co-Convenor Cochrane Prospective Meta-Analysis Methods Group
• Dr Kylie Hunter PhD MPH, Research Fellow at the NHMRC Clinical Trials Centre, Associate Convenor Cochrane Prospective Meta-Analysis Methods Group

Who should attend?

Anyone interested in learning more about using existing clinical trial data for secondary purposes, including, but not limited to:

• Higher Degree Researchers (HDRs) or PhD candidates
• Early Career Researchers
• Mid-late Career Researchers
• Infrastructure providers (including research facilities)
• Digital skills trainers
• Data custodians and/or data managers

Will the session be recorded?

Yes, the session will be recorded, provided to all registrants and published online.

About the ARDC People Research Data Commons

The ARDC People Research Data Commons (People RDC) is delivering national-scale data infrastructure for health research and translation.

Researchers, innovators and policymakers seek to improve health outcomes for society, and yet the data and digital platforms they need span multiple layers of government, health service operations, health research studies, institutes, facilities and the private sector. The People RDC initiative develops, operates and coordinates national-scale capabilities to support digital health research and translation.

Learn more and register your interest in the People RDC.

Further ARDC resources

• People Research Data Commons
• Health Studies Australian National Data Asset (HeSANDA)
• Health Data Australia
• ARDC website
• Resource Hub

Have Questions?

Email contact@ardc.edu.au.

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Please note that this event may 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.