Clinical Research Associate

Clinical Research Associate Job No.: 697931 Location: 509St Kilda Road campus Employment Type: Full time Duration: 12 months fixed-term appointment Remuneration: $110,527 – $121,227 pa HEW 07 (plus 17% employer superannuation) Amplify your impact at a world top 50 University Join our inclusive, collaborative community Be surrounded by extraordinary ideas - and the people who discover them The Opportunity The School of Public Health and Preventive Medicine is seeking a Clinical Research Associate to support the Transfusion Research Unit in delivering high-quality, investigator-initiated clinical trials. In this role, you’ll oversee trial activities from site set-up and staff training through to data monitoring, reporting and completion, contributing to high-impact research outcomes. Working closely with hospital sites, investigators and research partners, you’ll provide expert advice and coordinate essential clinical trial activities, including HREC and regulatory submissions, contracts, documentation and investigator meetings. You’ll also support the day-to-day delivery of trials, ensuring research protocols, quality standards and patient safety requirements are consistently met. We’re seeking an experienced clinical research professional with demonstrated clinical trial coordination experience and a current Good Clinical Practice (GCP) certificate. You’ll bring strong project management, analytical and organisational skills, along with the confidence to work independently, build effective stakeholder relationships and provide specialist advice across complex research activities. Previous experience conducting investigator-initiated trials and on-site monitoring visits will be highly regarded. About Monash University At Monash , work feels different. There’s a sense of belonging, from contributing to something groundbreaking – a place where great things happen. We value difference and diversity , and welcome and celebrate everyone's contributions, lived experience and expertise. That’s why we champion an inclusive and respectful workplace culture where everyone is supported to succeed. Learn more about Monash . Join the pursuit of our purpose to build a better future for ourselves and our communities - #ChangeIt with us. Monash supports flexible and hybrid working arrangements. We have a range of policies in place enabling staff to combine work and personal commitments. This includes supporting parents . To Apply For instructions on how to apply, please refer to ' How to apply for Monash Jobs '. Your application must address the Key Selection Criteria. Diversity is one of our greatest strengths at Monash. We encourage applications from Aboriginal and Torres Strait Islander people, culturally and linguistically diverse people, people with disabilities, neurodivergent people, and people of all genders, sexualities, and age groups. We are committed to fostering an inclusive and accessible recruitment process at Monash. If you need any reasonable adjustments, please contact us at hr-recruitment@monash.edu in an email titled 'Reasonable Adjustments Request' for a confidential discussion. Your employment is contingent upon the satisfactory completion of all pre-employment and/or background checks required for the role, as determined by the University. Enquiries: Vanessa Fox, Clinical Registries Program Manager, vanessa.fox@monash.edu ; or Enquiries: Naomi Aoki, Business Projects Manager, naomi.aoki@monash.edu Position Description: Clinical Research Associate Applications Close: Sunday, 20th September at 11:55pm AEST Supporting a diverse workforce Back to search results Email Job Apply now Monash University recognises that its Australian campuses are located on the unceded lands of the people of the Kulin nations, and pays its respects to their elders, past and present. Whatsapp Facebook LinkedIn Email App

• The School of Public Health and Preventive Medicine is seeking a Clinical Research Associate to support the Transfusion Research Unit in delivering high-quality, investigator-initiated clinical trials.
• In this role, you’ll oversee trial activities from site set-up and staff training through to data monitoring, reporting and completion, contributing to high-impact research outcomes.
• Working closely with hospital sites, investigators and research partners, you’ll provide expert advice and coordinate essential clinical trial activities, including HREC and regulatory submissions, contracts, documentation and investigator meetings.
• You’ll also support the day-to-day delivery of trials, ensuring research protocols, quality standards and patient safety requirements are consistently met.
• We’re seeking an experienced clinical research professional with demonstrated clinical trial coordination experience and a current Good Clinical Practice (GCP) certificate.
• You’ll bring strong project management, analytical and organisational skills, along with the confidence to work independently, build effective stakeholder relationships and provide specialist advice across complex research activities.
• Previous experience conducting investigator-initiated trials and on-site monitoring visits will be highly regarded.