Monday Lunch Live
20 May 2024
Designed for clinical trials staff involved in the consenting process, this webinar looks at enhancing equity in clinical trials through informed consent.
Divided into three parts, the webinar shares how consent is problematic, especially for some populations (CALD). It shares recommendations from an Early Phase Awareness project as well as the InFORMed project (CT:IQ), which helped reduce the consent form into something more equitable, accessible and manageable.
Chair
Dr Kortnye Smith
Medical Oncologist and Researcher, Peter MacCallum Cancer Centre and Eastern Health
After completing her mDredical oncology training, she pursued a two-year fellowship at Peter MacCallum Cancer Centre and the Melbourne Genomic Health Alliance where she investigated genomic sequencing in cancer therapy. Kortnye works predominantly in lung cancer and melanoma as well as focusing on her passion to improve patient equity by coordinating the Oncology in the Home program in Melbourne.
Dr Abhijit Pal
Dr Abhijit Pal specialises in Phase 1 cancer trials and thoracic malignancies. He completed a Phase 1 trials fellowship at the Drug Development Unit, Royal Marsden Hospital in London from 2019 – 2020. He was awarded a PhD in 2023 through the University of Sydney (supervised by Professor Frances Boyle), looking at informed consent for Phase 1 trials and ways to improve the representation of patients from culturally and linguistically diverse backgrounds on to cancer clinical trials.
Mr Duncan Colyer
Initially training as a nurse and working in Western Australia, he went to Oxford, UK in 2007 where he commenced his career in clinical trials. Returning to Australia in 2010, he worked at Peter MacCallum Cancer Centre as a Senior Research Nurse and Team Leader before changing his career to Program Management at the VCCC Alliance, focusing on clinical research. Duncan currently oversees the Programs of Clinical Trial Innovations and Accelerating Novel Therapies.
Dr Lisa Eckstein
Dr Lisa Eckstein was previously senior lecturer in the Faculty of Law at the University of Tasmania, where she chaired the Tasmania Health and Medical Human Research Ethics Committee. She has published on the regulation of clinical trials, genomic privacy, and consent.