Ethics Research Assistant

Monash Health is Victoria’s largest and most comprehensive health service. For more than 170 years, Monash Health and its predecessors have provided safe, high-quality healthcare and service for people at every life stage. To see first‑hand what our colleagues think about working here, take a look at the following short videos: monashhealth.org/careers . Join our team as an Ethics Research Assistant on a part time (24 hours/ 3 days), ongoing term to work at Haematology Research based at Clayton. About the role Assist in preparing and submitting the regulatory documentation to the Human Research Ethics Committee (HREC) and Research Governance (RGO) for clinical trials of the Haematology Research Unit. Draft and format study documents — e.g., Participant Information and Consent Forms (PICFs), investigator CVs, and study summaries, per ethics requirements. Coordinate and respond to HREC/RGO queries or requests for clarification, and track submission timelines. Support protocol amendments, site authorizations, annual reports, safety reports, and compliance documentation. Maintain accurate records and version control of all ethics and regulatory correspondence. Ensure study documents align with current regulations, policies, and templates. About us Monash Health Haematology has a large Clinical Trials Unit and utilises the purpose‑built state of the art Clinical Trials Unit at the Monash Health Translation Precinct to implement new and exciting clinical trial opportunities for our patients. Our Clinical Trials Unit currently runs ~120 clinical trials in all aspects of haematology, focussing on malignant as well as haemostasis/thrombosis trials, and offers patient‑centred care to patients with complex needs. This is a dynamic and fast‑paced team, working in an ever‑evolving developmental areas such as targeted therapy, immunotherapy, and chemotherapy. About you Bachelor’s degree in science, health, or related discipline. Sound knowledge of human research ethics, research governance, ICH‑GCP, NHMRC and clinical trial regulatory frameworks. Experience preparing or supporting HREC/RGO in a clinical trial setting. Excellent attention to detail, organisation, and document management skills. Strong written communication and ability to work with multidisciplinary research teams. Strong organisational and time‑management skills to meet multiple deadlines. Ability to work both independently and collaboratively within a research team environment. Proficiency in Microsoft Office and familiarity with online ethics submission portals (e.g., SSA, VSM). In Return You will join a collaborative and supportive research team working on high‑quality clinical trials that contribute to improving patient care. You will gain hands‑on experience across multiple projects, build strong relationships with investigators and research staff, and develop your expertise in clinical research ethics and governance within a dynamic and learning‑focused environment. For a confidential discussion and to explore the opportunity further, please email Purwani (************@monashhealth.org ). We recognise the value of equal employment opportunity. We are committed to patient safety, promoting fairness, equity and diversity in the workplace and to Child Safe Standards. At Monash Health we are relentless in our pursuit of excellence and work to our six guiding principles and our five ICare values. How to Apply Applications are accepted via the Monash Health onlineEHub system. For information including how to apply and probity check requirements, please click here for the ‘Application Guide’. Applications will be screened upon receipt and selection activity may commence prior to the closing date. #J-18808-Ljbffr