As Vice President and Head of Translational Science & Experimental Medicine for Cardiovascular, Renal and Metabolism (CVRM), I lead our human target validation, biomarker and precision medicine departments, working closely with team leaders in both early and late CVRM research. I help to direct our early-stage research priorities in CVRM and am involved in a multitude of initiatives across our early CVRM portfolio.
Our team’s collective ambition is to stop, reverse, and one day, cure CRVM diseases by delivering innovative, life-changing medicines and solutions to patients. Across our departments, patients are always the starting point of our work. To that end, the foundation of our research relies heavily on human clinical data and biological samples, rather than cellular or animal modelling.
I completed my PhD and MD at the University of Cambridge, Departments of Clinical Biochemistry and Medicine and am currently a practicing endocrinologist. The time I spend with patients shapes my understanding of their needs as well as the gaps they experience in existing healthcare systems. This is both rewarding and incredibly valuable to the work I do each day at AstraZeneca.
Working across industry and applied medicine, a key priority for me as department head is ensuring we have a clear purpose as a team. I encourage open communication of priorities to foster a collaborative and stimulating work environment where we can work together to push the boundaries of science to deliver life-changing medicines to our patients.
As a full-time consultant, I was not able to conduct the research that I was passionate about. What attracted me to AstraZeneca was the breadth and depth of their research programmes, particularly across CVRM diseases. My role now allows me to be at the forefront of cutting-edge clinical research, while still seeing patients as a practicing clinician; it’s both exciting and fulfilling.
CURRENT ROLE
2021 – present
2019 – 2021
2016 – 2019
2016 – present
Scientific publications
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank
Nag A., Dhindsa R.S., Middleton L. et al. Am J Hum Genet. 2023 Feb 10:S0002-9297(23)00046-0. doi: 10.1016/j.ajhg.2023.02.002.
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes
Nag A., Dhindsa R.S., Mitchell J. et al. Sci Adv. 2022 Nov 18;8(46):eadd5430. doi: 10.1126/sciadv.add5430.
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Wang Q., Dhindsa R.S., Carss K. et al. Nature. 2021 Sep;597(7877):527-532. doi: 10.1038/s41586-021-03855-y.
HEROIC: a 5-year observational cohort study aimed at identifying novel factors that drive diabetic kidney disease: rationale and study protocol
McCafferty K, Caplin B, Knight S et al. BMJ Open. 2020;10:e033923. doi: 10.1136/bmjopen-2019-033923
Veeva ID: Z4-54154
Date of preparation: April 2023