Ingrid King
Ingrid King
I am a Database Manager and Research Assistant specialising in cardiovascular research, with a focus on cardiomyopathy and pulmonary hypertension. I currently manage and oversee complex clinical research databases, including the Australian and New Zealand Pulmonary Hypertension Registry (PHSANZ), with affiliations at Royal Prince Alfred Hospital, Sydney, and the Royal Children’s Hospital.
My role encompasses database development and governance, REDCap database design and implementation, data quality assurance, and regulatory compliance. I work closely with clinicians, researchers, and governance teams to ensure accurate, high-quality data collection that supports impactful translational and clinical research locally and internationally.
In addition to database management, I contribute to ethics submissions, protocol development, registry coordination, collaboration agreements and research reporting. I am particularly passionate about building robust data infrastructure that advances cardiovascular research and improves patient outcomes.
My role encompasses database development and governance, REDCap database design and implementation, data quality assurance, and regulatory compliance. I work closely with clinicians, researchers, and governance teams to ensure accurate, high-quality data collection that supports impactful translational and clinical research locally and internationally.
In addition to database management, I contribute to ethics submissions, protocol development, registry coordination, collaboration agreements and research reporting. I am particularly passionate about building robust data infrastructure that advances cardiovascular research and improves patient outcomes.
I am a Database Manager and Research Assistant specialising in cardiovascular research, with a focus on cardiomyopathy and pulmonary hypertension. I currently manage and oversee complex clinical research databases, including the Australian and New...
I am a Database Manager and Research Assistant specialising in cardiovascular research, with a focus on cardiomyopathy and pulmonary hypertension. I currently manage and oversee complex clinical research databases, including the Australian and New Zealand Pulmonary Hypertension Registry (PHSANZ), with affiliations at Royal Prince Alfred Hospital, Sydney, and the Royal Children’s Hospital.
My role encompasses database development and governance, REDCap database design and implementation, data quality assurance, and regulatory compliance. I work closely with clinicians, researchers, and governance teams to ensure accurate, high-quality data collection that supports impactful translational and clinical research locally and internationally.
In addition to database management, I contribute to ethics submissions, protocol development, registry coordination, collaboration agreements and research reporting. I am particularly passionate about building robust data infrastructure that advances cardiovascular research and improves patient outcomes.
My role encompasses database development and governance, REDCap database design and implementation, data quality assurance, and regulatory compliance. I work closely with clinicians, researchers, and governance teams to ensure accurate, high-quality data collection that supports impactful translational and clinical research locally and internationally.
In addition to database management, I contribute to ethics submissions, protocol development, registry coordination, collaboration agreements and research reporting. I am particularly passionate about building robust data infrastructure that advances cardiovascular research and improves patient outcomes.
Top Publications
- Singer, ES, Smith, J, Lin, R, Morrish, AM, Lal, S, Irving, C, Casey, C, King, I, Weintraub, RG, Bagnall, RD. Case Report: Deletion in the 5' untranslated region of TAFAZZIN in a boy with Barth syndrome.. Front Cardiovasc Med 13: 1766067 2026 view publication
- Chang, Y, Wacker, J, Ingles, J, Macciocca, I, King, I, Australian Genomics Cardiovascular Disorders Flagship, Semsarian, C, McGaughran, J, Weintraub, RG, Bagnall, RD. TBX20 loss-of-function variants in families with left ventricular non-compaction cardiomyopathy.. J Med Genet 61(2) : 171 -175 2024 view publication
- Singer, ES, Crowe, J, Holliday, M, Isbister, JC, Lal, S, Nowak, N, Yeates, L, Burns, C, Rajagopalan, S, Macciocca, I, et al. The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death.. NPJ Genom Med 8(1) : 29 2023 view publication
- Bagnall, RD, Singer, ES, Wacker, J, Nowak, N, Ingles, J, King, I, Macciocca, I, Crowe, J, Ronan, A, Weintraub, RG, et al. Genetic Basis of Childhood Cardiomyopathy.. Circ Genom Precis Med 15(6) : e003686 2022 view publication
- Norrish, G, Topriceanu, C, Qu, C, Field, E, Walsh, H, Ziółkowska, L, Olivotto, I, Passantino, S, Favilli, S, Anastasakis, A, et al. The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy.. Eur J Prev Cardiol 29(4) : 645 -653 2022 view publication
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