What EMCRs Need to Know About Research Operations When Setting Up a Clinical Trial

Join the MISCH Clinical Trials Node, the Melbourne Centre for Clinical Trials and the University of Melbourne’s Office of Research Management for an informative seminar designed specifically for early‑ and mid‑career researchers.

We’ll unpack the key operational factors that underpin successful clinical trial setup, including governance requirements, budgeting, contracts, ethics submissions, data and safety processes, and operational workflows.

Attendees will gain practical insights into navigating the University’s system, working effectively with support teams, and avoiding common pitfalls when initiating a trial.

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About the Series: EMCR Research Design Webinars are conducted by experts from the University of Melbourne’s Methods and Implementation Support for Clinical and Health research Hub (MISCH), Melbourne Data Analytics Platform (MDAP), the Centre for Digital Transformation of Health (CDTH), and additional guest presenters.