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Alastair is a public policy scholar, a crisis management expert and has an ongoing interest in the institutionalization of participatory modes of governance. His current policy research examines the role that institutional amnesia plays in the policy process, his crisis management research has been focused upon the relationship between public inquiries and lesson-learning, and in relation to participatory governance, he is currently examining the validity of different forms of deliberative democracy in the context of Australian environmental policy. Alastair has published widely in high-ranking international journals and is the recipient of the Mayer Prize (best paper in the Australian Journal of Political Science) and the Lasswell Prize (best paper in Policy Sciences). He has authored three books, won three large-scale Australian Research Council Discovery grants and is always looking for outstanding students who may be interested in completing PhDs in relation to the topics outlined above.

Associate Professor Mitchell Stark is a molecular biologist and Group Leader (Principal Research Fellow) from the Dermatology Research Centre (DRC) based at the Frazer Institute, The University of Queensland (UQ; Brisbane, Australia). He leads the pre-melanoma genomics program at the Frazer Institute and his group has extensive experience in the use of next-generation sequencing, spatial transcriptomics, bioinformatics, and functional analysis for a variety of applications. The Stark Lab’s major research streams include: miRNA biomarkers for melanoma progression and the development a Genomics Atlas of pre-skin cancer lesions, which aim to provide to greater understand melanoma progression from naevi and early invasive melanoma, with a goal to discover novel predictive biomarkers that offer increased precision to the clinical management of patients.

He has been engaged in melanoma and nevus research for 25+ years (with 9-years post PhD) and over this time he has been working towards understanding the aetiology of melanoma, studying gene dysregulation during tumor progression along with predisposition to melanoma in families with high risk for melanoma development. Dr Stark has a total of 97 career publications including 1 book chapter, 83 journal articles, 12 reviews/perspectives and 1 patent (WO/2016/029260) which have been cited a total of 7,053/10,208 times (Scopus/Google; h-index: 38/42) and has published in respected journals such as Nature, Nature Genetics, Cancer Research, and Journal of Investigative Dermatology. He has been awarded a career total of ~$10M as an Investigator (PI/co-PI/co-Investigator) including a prestigious NHMRC Peter Doherty Early Career Research Fellowship (2016-2019) and a recent NHMRC Investigator award (2025-2029), along with several research grants as Principal Investigator (e.g., Advance QLD Innovation Partnership, Department of Defence CDMRP – Melanoma Research Program).

Dr Hana Starobova is a pharmacist and NHMRC research fellow at the Sensory Neuropharmacology Group at the University of Queensland (UQ). She works under the mentorship of Prof. Vetter, and as an early career researcher, she is working toward an independent research career as a group leader. She obtained her PhD in 2020 from the Institute for Molecular Bioscience, UQ, and continued here to conduct studies as a Children Hospital Foundation Fellow (2021-2023) in the areas of cancer therapy-induced adverse and late effects with the main focus on neuropathies. Over the past four years, she has developed a research program focusing on the understanding of cancer therapy-induced adverse and late effects with a special interest in children, and established innovative transcriptomic and microscopy pipelines, in vitro assays, adult and juvenile models of adverse and late effects following mono- and combination chemotherapy and radiotherapy, assays for the assessment of adverse effects including cognition and neuropathies, as well as cancer models. Knowledge impact arising from her research program has been disseminated in 18 peer-reviewed publications, having together attracted >1,100 citations (h-index 15, i10-index 18, Google Scholar, May 2024).

Dr Sally Staton is a Senior Research Fellow in the Science of Learning Research Centre at the Queensland Brain Institute, UQ. Dr Staton has a strong commitment to research that can inform and ensure positive early life experience for all children. Her research focuses on the role of early education and care settings in supporting young children’s immediate and on-going social-emotional, cognitive and physical development. Dr Staton’s research spans a range of study designs and methodologies, including evaluation studies in educational settings (applying randomised control trial and quasi-experimental designs), longitudinal studies tracking large child cohorts (>2000 children), standard observation techniques (in vivo and video), survey and individualised standard child assessment (using educational and psychological measures), as well as studies employing physiological (cortisol, actigraphy, heart rate variability) and qualitative (child, educator and parent interviews, socio-metric) designs. She has a particular expertise in the development, application and interpretation of observational measurement for educational practices and teacher-child interactions in education contexts, including early childhood settings. Dr Staton has a strong track record in research translation and community engagement, including delivery of reports for government and non-government organisations, professional development packages for early childhood professionals and teachers, presentations, workshops, videos and articles for parents, government regulatory officers and the early childhood sector. In 2016, she was named among Queensland’s Young Tall Poppy Scientists for her contribution to science translation and engagement. In 2019 her succesful research partnerships with industry and government was acknowledged in a Partners in Research Excellence Award from UQ.

I completed my Bachelor of Pharmacy at Kings College London, followed by pre-registration and subsequent employment as a pharmacist with Boots the Chemists in Central London. With a PhD in plant biochemistry with Royal Holloway College, University of London, and the Royal Botanic Gardens, Kew, I moved first to Cornell University, USA and then The University of Western Australia for postdoctoral research. I moved to the School of Pharmacy at The University of Queensland in 2007.

Following a number of years in plant research, my current research interests generally link back to plants in some way. Many of my projects develop in response to requests for help from healthcare professionals, and so I have a strong focus on answering clinical questions using pharmaceutical science methods. See my research interests for more information.

I teach into the Bachelor of Pharmacy (Honours) in the areas of pharmaceutics, compounding and complementary medicines. I also teach the clinical drug development course for our Master of Pharmaceutical Industry Practice. I am currently the Director of Teaching, Learning and Student Experience for the School of Pharmacy. I have supervised 28 PhD students to completion, and over 60 undergraduate and masters independent research project students.

My research is in the discipline of higher education and focuses on university teacher beliefs, thinking and practices in relation to the use of educational technologies in teaching & learning. I am also interested in learning designs to support authentic learning approaches using new and emerging technologies such as Web 2.0/3.0 technologies, mobile technologies and 3D immersive environments.

Caroline Steel’s research is in the use of current and emerging educational technologies primarily in university and more recently as applied to the field of Technology-Enhanced Language Learning. She is President and Executive Member of ascilite (Australasian Society for Computers in Learning in Tertiary Education). Her research into educational technologies draws on teacher and learner beliefs and affordance theories to investigate learner and teacher preferences and current uses of technology in education. She was lead researcher on a large multi-university research project that investigated the transitional experiences, motivational factors, technology preferences and uses of language students across 3 universities.

Caroline has worked in education-related fields for nearly 20 years as a language teacher, curriculum designer, university teacher educator and now research fellow. Caroline's PhD investigated university teachers' pedagogical beliefs, beliefs about web technologies and how these are enacted in practice. In her research she draws on a number of qualitative research approaches and methods including stimulated recall and concept mapping. Caroline teaches the Masters of Education course ‘Creating classrooms of the future with educational technology' and an undergraduate course in ‘Languages and Technology’.

Biography:

1992 - 1995. B.E. (Hons), Bachelor of Engineering (Chemical). The University of Melbourne.

1996 - 1999. Ph.D. (Engineering), Department of Chemical Engineering, The University of Melbourne.

2000 - 2008. Research Fellow then Lecturer. Nottingham Fuel and Energy Centre, School of Chemical and Environmental Engineering, The University of Nottingham, UK.

2009 - 2018. Lecturer then Senior Lecturer, School of Chemical Engineering, The University of Queensland.

2019 - present. Associate Professor, School of Chemical Engineering, The University of Queensland.

My research interests are in energy and resources, including coal science, gas recovery, and sustainable mineral processing with a strong interest in developing new technologies to solve major issues. I develop new experimental/analytical capabilities and innovative approaches to provide new knowledge and novel insights that can help Australian industries maintain and extend their competitiveness in world markets. I also develop novel process schemes by manipulating solution equilibria and are currently focused on developing new mineral processes that include CO2 sequestration.

Main themes:

Metallurgical Coal Carbonisation and Biocoke Production

I have pioneered the use of high temperature oscillatory shear rheometry to characterise the microstructure of coal during pyrolysis/carbonisation as it transforms into coke (an essential porous carbon material used for steel-making). I obtained real mechanical properties of the plastic phase that forms and studied viscoelastic thresholds for bubble nucleation, growth and coalescence which enabled me to develop a hypothesis for a process problem known as high oven wall pressure. The knowledge base created from this research has paved the way for better models to predict oven wall pressure and elucidated clever ways to control pressure through blending.

This led to an ambitious new focus to develop a mechanistic model for coke strength that would reveal why some coals are not well predicted and how the value of a coal could be improved through blending. I combine rheometry and X-ray micro-CT analysis to reveal the physical mechanisms by which the pore structure of coke forms and how its features contribute to coke strength.

More recently, I have turned my attention to examining how coal can be replaced by biomass in steel production given that 7% of the world’s CO2 emissions come from producing steel. This involves examining the pyrolysis behaviour of biomass and finding ways to replicate the mechanisms that give rise to strong coke. Initial work has involved sugar can bagasse, an agricultural waste, and therefore involves examining the behaviour of grasses.

Significance: Coal is the 2nd biggest export earner for Australia, whereby the majority is metallurgical (met) coal used to make coke, and Australia is currently the largest exporter of met coal in the world. My research is used to ensure Australia remains at the forefront by enabling better predictions on the behaviour of different coals and providing new opportunities for the marketing of Australian coals.

Main collaborators: ACARP, BHP, Anglo American, Rio Tinto, Peabody, Vale, The University of Newcastle (Aus), CSIRO, School of Earth Sciences (UQ).

Novel Technologies for Increasing Gas Recovery from Coal Seams and Predicting Gas Production Rates.

Methane is a ‘cleaner’ fuel than coal because it is hydrogen-rich and can be burned in high efficiency combined cycles. Coal deposits in eastern Australia have enormous amounts of adsorbed methane (known as coal seam gas or coalbed methane) which has given rise to a fast growing industry whereby the methane is extracted, liquefied (LNG), and exported overseas. Extraction depends on the permeability of the coal seam. The most commonly used technology for increasing permeability is hydraulic fracturing, which originates from the conventional oil/gas industry where sandstone is the usual source rock. The structural properties dictating permeability for coal is different, whereby coal is already highly cleated due to the shrinkage process that occurs during formation. Instead of creating a new fracture network, our research has shown that it is possible to increase gas productivity by working with the existing cleat network, enhancing flow by dissolving the minerals within the cleats and etching cleat surfaces.

I have developed new laboratory and analytical capabilities to study the chemical and physical effects caused during chemical injection, including X-ray micro-CT analysis combined with pore characterisation and flow simulation (using GEODICT) to explain the permeability changes observed in laboratory injection tests.

I have also recently developed a new tool that enables the cleats to be examined as methane is desorbed (using high pressure cells and X-ray CT analysis). We aim to relate our observations to the structural properties of the coal and provide industry with a new capability to predict gas production rates for a given well over its life. Approaches taken are also applicable to predicting flow and adsorption behaviour of CO2 for sequestration considerations. Once coal seams become depleted of methane, the same pore space that held the methane is available for long-term CO2 storage

Significance: Liquefied Natural Gas (LNG) is the 3rd biggest export earner for Australia. Industry is currently targeting regions where gas is easy to extract, and the challenge is to develop new technologies for increasing permeability in other regions and to predict gas production levels as a well depletes. My research supports industry by providing new technologies and new capabilities that helps them maintain and extend their position in the world market.

Main collaborators: Santos, Origin Energy, Arrow Energy, QGC, UQ Centre for Natural Gas, School of Earth Sciences (UQ).

Sequestration of CO2 as Stable Mineral Carbonates

Mineral carbonates are known to be stable for millions of years and so conversion of CO2 emissions to solid carbonate is an attractive solution. My background in manipulating solution equilibria to achieve desired effects led me to establish novel chemical routes for making Mg-carbonates from CO2 and either Mg-silicates or Mg-rich tailings. Given that Mg-silicates can contain Ni the process can be aligned with the current process for Ni recovery. Furthermore, the process can extract CO2 from the atmosphere and can therefore offset the release of CO2 elsewhere.

Significance: Technologies to mitigate against CO2 emissions are of unparalled importance. One of the major challenges is keeping the cost low. Using clever chemistry and combining CO2 sequestration with existing mineral processing operations that produce valuable commodities could enable it to work commercially.

Julian A. Steele received his Ph.D. in physics from The Institute for Superconducting and Electronic Materials (ISEM), University of Wollongong, before undertaking postdoctoral work at KU Leuven (Belgium) and UC Berkeley (USA). From 2023, he began a DECRA Fellowship at the Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, working on a range of condensed matter topics, within which phase transition phenomena in metal halide perovskite semiconductors feature heavily.

Nik is Associate Professor and Director of the Centre for Business and Organisational Psychology (CBOP) in UQ's School of Psychology. He lived, worked, and studied psychology in Germany and Spain and completed his PhD in the UK before working at The University of Queensland (Australia).

Nik conducts fundamental and applied research to uncover psychological drivers that make groups and organisations fairer, more motivating, more effective, and healthier. His expertise lies in social identity and team work processes in social and organisational contexts including leadership and followership, motivation and creativity, and health and well-being. He uses diverse methods to understand people and organisations including experimental and intervention studies, field and survey research, archival methods, psychometric scale development, and systematic reviews and meta-analysis.

His work has been supported by several bodies including the Australian Research Council (e.g., he was awarded an ARC DECRA fellowship in 2018), the Australian Government, and several industry research-partnerships (with public and private organisations). In 2017, he won the APS Workplace Excellence Award for Leadership Development (together with Alex Haslam and Kim Peters) for his work with industry partners on the 5R leadership development program that seeks to help leaders to develop their leadership ability and enhance team functioning and well-being (https://tinyurl.com/adfu7xbu). He consults to organisations around social and organisational challenges and he is an (IECL-certified) orgnisational coach.

Nik is a co-founding member of the Global Identity Leadership Development (GILD) network of global leadership scholars, and serves on the Editorial Board of the European Journal of Social Psychology, and the flagship journal for leadership research, The Leadership Quarterly. He is Editor (with Michelle Ryan and Floor Rink) of the 'Organisational Psychology: Revisiting the Classic studies' published in 2023 as part of SAGE's classic studies in psychology series (https://us.sagepub.com/en-us/nam/organisational-psychology/book269849).

Dr Stehbens is a cell biologist with a long-standing interest in understanding the fundamental mechanisms that regulate cell adhesion and the cytoskeleton. She has made key contributions to the fields of quantitative microscopy, cell motility, adhesion and the cytoskeleton with publications spanning multiple fields from ion channels in brain cancer, to growth factor signalling and autophagy. Her research group (joint between AIBN and IMB) aims to understand the fundamental principles of how cells integrate secreted and biomechanical signals from their local microenvironment to facilitate movement and survival. They have uncovered an entirely novel role for the microtubule cytoskeleton in protecting cells from cortical and nuclear rupture during cell migration in 3D cell migration and invasion. Using patient-derived tumour cells, coupled to genetic alteration and substrate microfabrication, they use state-of-the-art microscopy to understand the mechanisms of cell migratory behaviour required for cancer cells to traverse the body during metastasis.

Her graduate work in the laboratory of Alpha Yap (IMB IQ) discovered how the microtubule cytoskeleton regulates cell-cell adhesion. After which she relocated to The University of California San Francisco (UCSF) to work with Prof Wittmann, a microtubule biologist who is an expert in live-cell spinning disc microscopy. Here she worked at the cutting edge of biology imaging advancements as the greater bay area research community combines several of the top-laboratories for imaging technologies. Supported by a competitive American Heart Fellowship Post-Doctoral fellowship, she identified how microtubules coordinate protease secretion during migration to mediate cell-matrix adhesion disassembly. In 2013, she returned to Australia to expand her imaging-based skill set to focus on models of cancer cell biology. Working with Prof. Pamela Pollock (QUT) she uncovered how activating FGFR2 mutations resulted in a loss of cell polarity potentiating migration and invasion in endometrial cancer. Following this, she worked with Prof. Nikolas Haass (UQDI) a melanoma expert, investigating the role of microtubule +TIP proteins in 3D models of metastatic invasion before starting her lab at the Institute for Molecular Bioscience as an ARC Future Fellow.

Lab Overview

Cells in living organisms navigate highly crowded three-dimensional environments, where their coordinated migration provides the driving force behind developmental and homeostatic tissue maintenance. Our research aims to understand the fundamental principles underpinning how cells integrate secreted and biomechanical signals from their local microenvironment to facilitate cell movement and survival. We apply these findings to understand how cancer cells exploit this to metastasise or spread to distal tissues. We hypothesise that targeting the crosstalk between the cytoskeleton and the mechanical micro-environment, can be developed as an anti-metastatic approach.

Cancer cells spread aggressively through tissues by adapting their cell shape to fit the environment in addition to altering their environment so they can squeeze through tight tissue spaces. Cancer cells sense and become more invasive following changes in the biophysical properties their microenvironment including increases in stromal stiffness and interstitial fluid pressures. These changes make cancer cells mechanically compliant and adaptive to fluctuations in their surrounding environment allowing them to alter their shape to fit matrix physical attributes. As such, cells need mechanisms in place to 1) detect these physical limits, 2) deform their cortex whilst producing mechanical force for forward locomotion and 3) orient themselves to move through tissues. We focus on understanding- at the molecular level- how the microtubule cytoskeleton and microtubule associated proteins called +TIPs, regulate how cells move through physically challenging environments. To do this we utilize cutting-edge methodology including microchannel fabrication, novel light sheet microscopy, quantitative imaging methods in combination with patient-derived cell and 3D hydrogel models to recapitulate the 3D microenvironment.

Our research areas include:

• Cytoskeleton
• Cell adhesion
• Cell migration
• Cell mechanics
• Cancer cell biology

Areas of Expertise

Microtubules and Cell-Cell Adhesion

My early research, in the laboratory of Professor Alpha Yap, focused on understanding how the microtubule cytoskeleton regulates E-cadherin-based cell-cell adhesion. This work was the first to discover that it was the dynamacity, not simply the tethering, of the microtubule cytoskeleton that was critical for E-cadherin accumulation and junctional reinforcement. This was in addition to defining a previously unappreciated role for the cytokinetic machinery (Ect2) in regulating cell-cell adhesion

• Stehbens, S.J., …,and Yap, A. S. (2006). Dynamic Microtubules Regulate the Local Concentration of E-cadherin at Cell-Cell Contacts. Journal of Cell Science 119: 1801-1811
• Ratheesh, A., … Stehbens, S.J., and Yap, A.S. (2012). Centralspindlin and α-catenin regulate Rho signalling at the epithelial zonula adherens. Nature Cell Biology 14(8): 818-28

Microtubules and Cell-Matrix Adhesion

Following my PhD, I relocated to the University of California San Francisco to work with Professor Torsten Wittmann, an expert in live-cell spinning disc microscopy and microtubule functions during cell motility. This work was dogma changing and established how the microtubule interacting protein, CLASP, facilitates targeted protease secretion at focal adhesions during epithelial sheet migration to mediate cell-matrix adhesion disassembly, from the inside-out. It includes the first observation of live, directed exocytosis of the matrix protease MT1MMP at focal adhesions. Our work pioneered the combined application of quantitative live-cell protein dynamics and the application of the novel super resolution imaging technique, SAIM (Scanning Angle Interference Microscopy). During my time at UCSF I learnt how to custom design live-cell microscopes with these live-cell imaging platforms now commercially distributed as the Spectral Diskovery and Andor Dragonfly.

• Stehbens, S.J., … and Wittmann., T (2014). CLASPs link focal-adhesion-associated microtubule capture to localized exocytosis and adhesion site turnover. Nature Cell Biology 16(6): 558-570
• Stehbens, S.J., and Witmann, T. (2014) Analysis of focal adhesion turnover: a quantitative live-cell imaging example. Methods in Cell Biology 123: 335-46
• Stehbens, S.J., and Witmann, T. (2012) Targeting and transport: how microtubules control focal adhesion dynamics. Journal of Cell Biology 20, 198(4): 481-9

Cell Morphology and Cancer Biology

In 2013 I returned to Australia, joining the lab of Pamela Pollock with focus on applying my skill set to have translational impact. Here I described the impact of activating FGFR2b-mutations on endometrial cancer progession. These findings uncovered collective cell polarity and invasion as common targets of disease-associated FGFR2 mutations that lead to shorter survival in endometrial cancer patients.

Stehbens, S.J, Ju, R.J and Pollock P.M. (2018) FGFR2b activating mutations disrupt cell polarity to potentiate migration and invasion in endometrial cancer. Journal of Cell Science, 131(15)

Microtubules in Metastatic Plasticity

In 2017, I joined the Experimental Melanoma Group at UQDI, where I work together with Professor Nikolas Haass in applying innovative live-cell spinning disc confocal imaging and biosensor approaches to understand cell-cell and cell-matrix interactions of melanoma with its microenvironment. Our work explores the adaptive role that the microtubule cytoskeleton plays in facilitating cell shape plasticity, matrix remodelling and resistance to compression during migration in complex 3D matrix models of metastatic melanoma invasion. We are fundamentally interested in understanding the reciprocal biophysical relationship between the microtubule cytoskeleton and the microenvironment during melanoma invasion, with the aim to expand our findings to other metastatic cancers.

Ju, Robert J., Stehbens, Samantha J., Haass, Nikolas K. 2018, ‘The Role of Melanoma Cell-Stroma Interaction in Cell Motility, Invasion, and Metastasis’, Frontiers in Medicine, vol. 5

Assoc. Prof. Stephan is an anatomist and forensic anthropologist with research interests in skeletal analysis and identification in the medicolegal setting. Specifcally these research interests include: craniofacial identification, radiographic comparison, trauma, unmingling of skeletons, biological profile estimations and standards of practice. Carl heads the Laboratory for Human Craniofacial and Skeletal Identification (HuCS-ID Lab), and is Chief Anatomist at The University of Queensland (UQ) School of Anatomy.

Carl is a Fellow of The American Academy of Forensic Sciences and recent past President of the International Association of Craniofacial Identification. Carl served as Special Issue Managing Guest Editor for Forensic Science International, Latest Progress in Craniofacial Identification, 2018. He has been Editorial Board Member of the Journal of Forensic Sciences (2013-23) and Associate Editor of Forensic Anthropology (2016-20). Carl founded the SBMS Skeletal Collection and Skeletisation Program at UQ in late 2014, re-energising forensic osteology within the UQ School of Anatomy and more broadly within the School of Biomedical Sciences.

Carl's prior appointments include forensic anthropology analyst with the Iraq Mass Graves Investigation Team (USA Army Corps of Engineers on behalf of the USA Department of Justice) and ORISE researcher at the USA Department of Defence Central Identification Laboratory in Hawaii. He often now serves as an external consultant to the USA Defence POW/MIA Accounting Agency (DPAA). At UQ and as Chief Anatomist and School of Anatomy manager, Carl works very closely with the SBMS Gross Anatomy Facility, in all matters of anatomy teaching, research and governance management.

Working in joint with the GAF Manager, Carl has cross adapted ISO17025 style practices and auditing procedures to the UQ School of Anatomy space and introduced the first Code-of-Practice for Use of Human Tissues within the UQ School of Anatomy since its inauguration (1927). These accreditation-style policies and procedures are further implemented and expanded in the HuCS-ID Lab, providing vital learning experiences and skill sets for Honours and Higher Research Degree students wanting to pursue careers in forensic science. New data analytic, casework and research tools developed by the HuCS-ID Lab and in the statistical environment of R, are freely and routinely released for others to use at the website: CRANIOFACIALidentification.com.

Carl's research outputs currently exceed 100 total scientific publications, including more than 85 full-length research articles..

Elizabeth Stephens is an Associate Professor of Cultural Studies in the School of Communication and Arts. She was previously an Australian Research Council Future Fellow in the Institute for Advanced Studies in the Humanities (UQ, 2017-2021), Associate Dean Research at Southern Cross University (2014-2017), and an ARC Australian Research Fellow in the Centre for the History of European Discourses (UQ, 2010-2014). Her background is in gender and sexuality studies, and her current research focuses on three interconnected themes:

• popular histories and representations of science, medicine and technology
• collaborations between the arts and sciences
• the critical medical humanities

A new research project examines the history and culture of work, productivity and fatigue. Elizabeth is author of over 100 publications, including four books: Artificial Life: The Art of Automating Living Systems (University of Western Australia Press, 2025), co-authored with Oron Catts, Sarah Collins, and Ionat Zurr, A Critical Genealogy of Normality (University of Chicago Press, 2017), co-authored with Peter Cryle; Anatomy as Spectacle: Public Exhibitions of the Body from 1700 to the Present (Liverpool University Press, 2011), and Queer Writing: Homoeroticism in Jean Genet's Fiction (Palgrave 2009).

She welcomes inquiries from potential PhD students, and can offer supervision in the following areas:

• cultural studies of science, medicine and/or technology
• art/science collaboration
• medical humanities
• digital cultures
• gender and sexuality studies

I began my scientific career with a Bachelor of Science in Biochemistry and Chemistry, followed by a Bachelor of Science with First Class Honours in Chemistry from Massey University, New Zealand. My honours project focused on developing hydrogels for controlled peptide release in the gut. I then pursued a PhD at Massey University, working on synthetic anti-cancer drugs based on cyclodextrins.

After completing my PhD, I worked as a Research Officer at the New Zealand Veterinary Pathology Epicentre, refining my diagnostic research skills. I continued my career as a Postdoctoral Fellow at Kansas State University, contributing to the detection and surveillance of zoonotic diseases in the swine industry.

Currently, at the University of Queensland, I integrate my expertise in synthetic peptides with vaccine development. My research bridges medical and agricultural biotechnology, focusing on innovative adjuvants and vaccines that span medicinal chemistry, nanotechnology, and immunology, aiming to enhance both health outcomes and agricultural practices.

Michele Sterling is a NHMRC Leadership Fellow (leadership level 2), Professor in the Recover Injury Research Centre, Program Lead of the Musculoskeletal Injury research program and Director of the NHMRC Centre of Research Excellence (CRE) in Better Health Outcomes for Compensable Injury. She is a Musculoskeletal Physiotherapist and a Fellow of the Australian College of Physiotherapists. She is internationally recognised for her research on whiplash-associated disorders. Michele’s research focusses on the mechanisms underlying the development of chronic pain after injury, predictive algorithms for outcomes and developing effective interventions for musculoskeletal injury and pain. She has received over $50M in research funding from the NHMRC, MRFF, ARC and industry partners, including 7 NHMRC project grants, and 2 Centres of Research Excellence. Michele holds editorial roles with several leading journals and textbooks, including being a Section Editor of PAIN and co-editors of the 4th and 5th editions of the seminal physiotherapy textbook 'Grieve's Musculoskeletal Physiotherapy). Michele has published over 325 scientific works and has received numerous awards for her research including the Research Australia Research Translation award in 2023. Examples of recognition as a national and international leader in the field include:

2024- Secretary of the Executive Council - International Association for the Study of Pain (IASP)

2022-2024 Chair Scientific Program Committee World Pain Congress, Amsterdam 2024

2023-2027 NHMRC Leadership Fellow (Level 2) for research of road traffic injury.

2023 Research Australia Research Translation award

2016-2022 Council member International Association for the Study of Pain (IASP)