Board of Directors
Hepatitis Victoria is overseen by a Board of Directors. The Board consists of:
- seven elected members;
- one person from a community organisation representing the interests of people who inject drugs;
- one person representing the interests of culturally diverse people;
- one person representing the interests of Aboriginal people;
- one person representing the interests of people from rural Victoria;
- one person with special skills or expertise required by Hepatitis Victoria as determined by the Board; and
- the Chief Executive Officer of Hepatitis Victoria (non-voting position)
Election of Board members takes place at the Annual General Meeting.
Frank Carlus (President)
Frank is a former state public servant with over 32 years’ experience in the Department of Human Services/Department of Health. In that time he worked in direct care, policy and senior management positions across a range of services.
Dr Nicole Allard (Vice-President)
Nicole is a GP in a community health centre. Her areas of interest include refugee health, hepatitis B community care, and working with CALD communities. She has initiated a hepatitis B clinic with support from the Integrated Hepatitis B service at the Royal Melbourne Hospital.
Kieran Donoghue (Treasurer)
Kieran is General Manager, Policy at an industry advocacy organisation. Prior to this he qualified as a chartered accountant with Deloitte in London and spent several years in a variety of finance roles at international companies.
Ross Williams (Secretary and Public Officer)
Ross worked as a psychology academic until he was diagnosed with hepatitis
C in 2006. Two liver transplants and four interferon treatments later,
today the virus is no longer detectable. Ross brings his strong
interest in issues in treatment and transplantation.
Todd is undertaking his doctorate at the University of Melbourne whose research focuses on how Aboriginal health services respond to sexuality and gender. For over a decade he has worked within the health and research sector. Todd is a descendant of the Kalarie Peoples of the Wiradjuri Nation.
Jarrod is a primary care pharmacist with a specific interest in liver health, harm minimisation, and reducing stigma in healthcare.
Melanie Eagle (Non-Voting CEO)
With formal qualification in Law, Arts and Social Work Melanie has worked in the public and private sectors including in the areas of future city strategic planning, social policy and women’s policy, equal opportunity, and as a private sector solicitor.
Paul has been living with HIV for 30 years and hepatitis C for 15. A writer, educator and activist, he has extensive community governance experience. He is a past President of Living Positive Victoria.
Eddie is currently Deputy Chair of the Ethnic Communities Council of Victoria, Chair’s the ECCV Health Committee and their Drugs Task Force and is a member of the Inner South Community Health Centre Board of Management. Previously a Victorian parliamentarian he was a member of its Drugs and Crime Committee.
Jennifer is an epidemiologist with the WHO Collaborating Centre for Viral Hepatitis, Victorian Infectious Diseases Reference Laboratory based at The Doherty Institute, Melbourne. She has postgraduate degrees in biological science and epidemiology, and has helped develop clinical guidelines and government policy at a state, national and international levels.
Phoebe is a nurse specialising in liver disease in both the acute and community settings. Phoebe has a background in international health and is passionate about delivering health care that is therapeutic, accessible and sustainable.
is currently the Director of Clinical Services at Uniting Care
ReGen. She has
extensive experience in the health sector including in hospitals in Australia
and overseas, including mental health services – and is a registered nurse
(general and psychiatric.
Ian brings 20 years’ management experience in Community sector. He has worked predominantly with hard to engage/ complex client groups within the homeless sector in both metropolitan and regional settings.