Unlock the Potential of Secondary Data from Clinical Trials with Health Data Australia

About the Event

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 guides you to uncover strategies to optimise your approach to using secondary clinical trial data and maximise the impact of your work.

Watch the recording

Speakers

• 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, NHMRC Clinical Trials Centre, and 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.

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.

Do you have questions about this event? Contact us.