As the Executive Director and Head of Renal Bioscience, Cardiovascular, Renal and Metabolism (CVRM) and a member of the CVRM Review Board, I lead AstraZeneca’s early research strategy on kidney diseases and work closely with our commercial and late-stage development teams.

By leading our early-stage renal research strategy, I help to ensure that we use patient-first thinking and build our scientific understanding of these diseases to identify and validate treatment targets that address unmet clinical needs. I am accountable for delivering new drug targets to the renal portfolio and work with my team to identify and validate novel targets and pathways of interest. My responsibilities include integrating the latest technologies – including artificial intelligence (AI) and digital health solutions – into our research, and presenting potential drug targets for review, to ensure we are always focused on projects with the greatest potential to improve the lives of patients.

My academic career began with my PhD at the University of Southern Denmark, focusing on vascular resistance in renal blood vessels using in vitro techniques. Over the following 15 years, I undertook postdoctoral research at the National Institutes of Health (NIH) before returning to the University of Southern Denmark where I taught and came to lead a research group. I have acquired extensive experience studying the kidney using in vitro, in vivo and translational approaches and since joining AstraZeneca, I have helped to bridge academic and industry interests. This has led to collaborations with the Karolinska Institutet and Harvard Medical School, among others. I am also leading an partnership with Benevolent AI to integrate its AI capabilities with AstraZeneca’s scientific excellence to deliver novel targets for chronic kidney disease (CKD).

Alongside my role at AstraZeneca, I hold academic positions as Professor at University of Southern Denmark and Gothenburg University. My scientific interests are kidney pathophysiology, kidney function and blood pressure regulation. The evidence from our research formed the basis for translational research that is informing novel advances in understanding kidney disease.

My drive to transform our understanding of kidney disease biology includes focusing on areas of widespread, unmet patient need, such as CKD, where diagnosis often comes later and treatments are not available to stop the progression of disease. It continues to be an incredibly rewarding challenge to pioneering the science, explore new scientific areas and lead groundbreaking research.

Pernille B. Laerkegaard Hansen Executive Director and Head of Bioscience Renal, Cardiovascular, Renal and Metabolism (CVRM), AstraZeneca

Scrip Awards

Best Partnership Alliance, with Benevolent AI (2021)

Danish Hypertension Society

Novartis Research Award (2010)

National Institutes of Health (NIH)

Fellows Award for Research Excellence (2004)

Pernille B. Laerkegaard Hansen, Executive Director, Head of Bioscience Renal, CVRM.

Key Achievements

Executive Director and Head of Bioscience Renal, Cardiovascular, Renal and Metabolism (CVRM), AstraZeneca

2016 – present

Executive Director, Head of Bioscience Renal, Cardiovascular, Renal and Metabolism (CVRM), AstraZeneca, responsible for the early-stage renal pipeline bringing projects from target identification to clinical trials. I am part of the CVRM review board, leading teams in the discovery phase for kidney diseases.

2019 – 2022

Project lead for AstraZeneca/Benevolent AI Chronic Kidney Disease (CKD) collaboration, with the aim to discover new drug targets for CKD employing knowledge graphs and machine learning.

2013 – present

Professor at University of Southern Denmark, extending my research through academia, exploring vascular function both in normal physiological settings, and in cardiovascular and renal diseases. My key research areas of focus are calcium channels, adenosine and aldosterone and their involvement in cardiovascular and renal physiology and pathophysiology.

Scientific publications


Selecting the right therapeutic target for kidney disease

Buvall L, Menzies RI, Williams J et al. Front Pharmacol. 2022 Nov 2;13:971065. doi: 10.3389/fphar.2022.971065.

Rare variant contribution to human disease in 281,104 UK Biobank exomes

Wang, Q., Dhindsa, R.S., Carss, K. et al. Nature 597, 527–532 (2021). DOI:10.1038/s41586-021-03855-y

Improving productivity with better predictivity

LC. Ewart, RJ. Goodwin, SE. Fawell, et al. Drug Discovery World 18-24, 2018

Editorial overview: Cardiovascular and renal: Blood pressure regulation and hypertension –hunt for new treatment targets in the kidneys

Pernille BL Hansen, Boye L Jensen. Curr Op Pharmacol, Volume 21, 2015, Pages v-viii, ISSN 1471-4892DOI: 10.1016/j.coph.2015.02.005.

Functional and pharmacological consequences of the distribution of voltage-gated calcium channels in the renal blood vessels

Hansen PB. Acta Physiol (Oxf). 2013 Apr;207(4):690-9. DOI: 10.1111/apha.12070.

Functional importance of L- and P/Q-type voltage-gated calcium channels in human renal vasculature

Hansen PB, Poulsen CB, Walter S, et al. Hypertension. 2011 Sep;58(3):464-70. DOI: 10.1161/HYPERTENSIONAHA.111.170845.

Adenosine induces vasoconstriction through Gi-dependent activation of phospholipase C in isolated perfused afferent arterioles of mice

Hansen PB, Castrop H, Briggs J, et al. J Am Soc Nephrol. 2003 Oct;14(10):2457-65. DOI: 10.1097/01.asn.0000086474.80845.25.

Differential expression of T- and L-type voltage-dependent calcium channels in renal resistance vessels

Hansen PB, Jensen BL, Andreasen D, et al. Circ Res. 2001 Sep 28;89(7):630-8. DOI: 10.1161/hh1901.097126.

Veeva ID: Z4-52040
Date of preparation: February 2023