The team accountable for every trial we deliver.

Over 160 people. 
One shared standard  of execution.

We carry institutional knowledge of every program we work on, from the first protocol conversation to final database lock. When a protocol stays within one team from design to execution, accountability becomes a personal guarantee.

Leadership Team

Meri Beckwith
Co-CEO
Meri is a former life sciences and healthtech venture capital investor, with an MSc in Biology from the University of Oxford. Serving on the boards of health and biotech companies, he saw CROs repeatedly fail to deliver clinical trials on time and on budget. After participating in a COVID-19 vaccine trial, he saw how fragmented integrated technology, poor patient experience and operational problems at sites cascaded up to the cost and timeline overruns he experienced as an investor. He founded Lindus to fix these problems and provide a more accountable, predictable model for research.
Michael Young
Co-CEO
Michael was previously a Special Adviser to the UK Prime Minister, where he advised on a range of issues including life sciences. Before serving in government, he worked at McKinsey & Company and L.E.K. Consulting, predominantly on commercialization and strategy in the healthcare space. His time in government during the pandemic showed him how much trial delivery depended on fragmented, outdated infrastructure, and convinced him the industry needed a fundamentally different operating model; without this none of the groundbreaking advances in understanding human biology will ever benefit patients. He founded Lindus to fix these bottlenecks.
Gemma Harrison
Chief Product & Technology Officer
Gemma leads R&D of CitrusTM, Lindus’ AI-native operating system. She is a technology executive who has spent her career building and scaling engineering teams. Before Lindus she spent three years as a Principal Software Engineering Manager at Microsoft, leading teams of up to 30 engineers on Telecoms products in Azure. Prior to that she spent 23 years at Metaswitch Networks, advancing from Software Engineer to Senior Software Engineering Manager. She holds a BA in Mathematics and a Diploma in Computer Science from the University of Cambridge, and is an active advocate for women in technology.
Heather Davis
VP of Clinical Operations
Heather has over 30 years of experience in clinical operations, spanning clinical site, biotech, and CRO environments. She co-founded Highline Sciences, an oncology-focused CRO, and served as its COO, scaling the company from seven employees to over 100 before its acquisition by Tempus AI. She remained as COO of Tempus Compass, integrating technology with clinical operations and supporting the company through its IPO. Her earlier career includes senior roles at Precision For Medicine, SynteractHCR, and Novella Clinical (now IQVIA), across oncology, immunology, and neurology.
Dr. Luke Twelves
VP of Medical
Luke is a physician with nearly three decades of clinical and leadership experience. He was Lindus employee number three. He previously served as CEO of Omnes Healthcare, delivering dermatology, ENT, diagnostic, and general practice services to the NHS, and directed clinical governance at UnitedHealth Group (Optum). He continues to practise as a GP alongside his role at Lindus, bringing frontline clinical perspective to the medical oversight of every trial. He trained at the Universities of Oxford and Cambridge, and holds an MBA from Durham University.
Richard McCormick
VP of Clinical Solutions
Rich is a clinical research executive with over two decades in oncology trial management. He built his foundation during an 11-year tenure at PPD, progressing from Research Associate to Project Manager across global oncology programmes. He went on to lead immuno-oncology project management at IQVIA Biotech, then held senior roles at Novella Clinical (now IQVIA), KCR, Vial, and ICON Biotech. His career spans Phase I through Phase IV oncology studies, with particular depth in immuno-oncology clinical strategy and global trial oversight.
Veronica Vu
VP of Deployment
Veronica is a clinical data management leader with over a decade of experience in designing and delivering clinical trials. At Lindus, she built and scaled the global Deployment team - leading the design, configuration, and UAT of new clinical trials on CitrusTM, Lindus’ AI-native operating system. Previously, she led data and delivery teams at Verily Life Sciences, where she was the data management lead for their first decentralized drug trial, and at Faro Health, where she shaped the data management strategy within the Product organization.

Advisory Board

Lindus is supported by a board of expert advisors spanning clinical development, regulatory affairs, biotechnology, and therapeutic area specialized medicine. Their depth of experience informs the standards we hold ourselves to.

Strategic Advisors

Robert Langer
Robert S. Langer, ScD, co-founded Moderna and over 40 other biopharma companies. He holds 1,400+ patents licensed to 400+ pharmaceutical, biotech, and medical device companies, and is one of three living individuals to have received both the US National Medal of Science and the National Medal of Technology and Innovation. He is an Institute Professor at MIT — the institution's highest faculty honour — and a member of the Koch Institute for Integrative Cancer Research. He is the most cited engineer in history, with over 1,600 published papers.
Dr. Tim Garnett
Tim spent 23 years at Eli Lilly, serving as Chief Medical Officer and Senior Vice President from 2008 to 2021. He oversaw regulatory affairs, patient safety, and clinical development across the US, Europe, China, and Japan, and led the global development of duloxetine across depression, pain, and incontinence indications. He also managed the raloxifene (EVISTA) programme in women's health. He currently chairs the board of Ophirex and serves as a board member for MapLight Therapeutics and Cardiol Therapeutics.
Dr. Alessandro Falcone
Alessandro is a medical doctor and life sciences executive currently serving as Regional Head of JLABS Singapore for Johnson & Johnson. At AstraZeneca, he served as Executive Director of Breast Cancer Oncology R&D Clinical Development Strategy, leading clinical programmes for three marketed oncology therapies: Enhertu, Lynparza, and Imfinzi. He previously held R&D leadership roles at GSK and strategy roles at Novartis. He holds an MBBS from UCL and an MSc in Experimental and Translational Therapeutics from the University of Oxford.

Scientific Advisors

Dr. Michelle Griffin
OB/GYN
Michelle is the founder of MFG Health Consultancy, where she partners with women's health founders to take innovations from concept to commercial success, helping secure over $85 million in investment. She led the NHS implementation of Stella, a clinically validated app for menopause treatment, and is the author of Fibroids (Penguin Random House). Her clinical career spans obstetrics and gynaecology, Cancer Research UK, and a WHO fellowship developing Zika virus management protocols for pregnant women.
Carel le Roux
Cardiometabolic
Carel is the Director of the Metabolic Medicine Group at University College Dublin. He served as principal investigator on the Boehringer Ingelheim Phase 2 survodutide trial — a glucagon/GLP-1 receptor dual agonist for obesity — published in The Lancet Diabetes & Endocrinology. He is a co-investigator on the SYNCHRONIZE Phase 3 programme and the TRIUMPH retatrutide trials in obesity and obstructive sleep apnea. He has over 350 publications with 22,000+ citations across obesity, type 2 diabetes, and gut hormone research.
Peter G. Polos, MD, PhD
Respiratory
Peter is a practicing pulmonologist and Associate Professor at Hackensack Meridian JFK University Medical Center. As Principal of Global Clinical Consulting, he has led clinical development and medical monitoring across 50+ Phase I–IV studies in asthma, COPD, and sleep medicine. He spent eight years as Global Director of Scientific Affairs at Merck, where he contributed to the montelukast (Singulair) clinical programme. He is a Fellow of both the American College of Chest Physicians and the American Academy of Sleep Medicine.
Chris Butler
Primary Care and Infectious Diseases
Chris is Professor of Primary Care at the University of Oxford and Clinical Director of the Primary Care Clinical Trials Unit. He has led or co-led over 30 randomised clinical trials recruiting 40,000+ participants, including the PRINCIPLE and PANORAMIC adaptive platform trials for COVID-19 community treatment, evaluating nine medicines. He has published over 500 papers across respiratory infections and COPD, with results in The Lancet, The BMJ, and the New England Journal of Medicine. His H-index exceeds 80.
Paul Billings, MD, PhD
Diagnostics
Paul was Chief Medical Officer at Natera, a global leader in cell-free DNA testing, where he oversaw diagnostic programmes across reproductive health and oncology. He also led Biological Dynamics as CEO, a liquid biopsy diagnostics company focused on early-stage cancer detection. He has authored over 250 publications on genomic medicine and held academic appointments at Harvard, UCSF, Stanford, and UC Berkeley. He sat on the FDA's Science Board and the HHS Secretary's Advisory Committee on Genetics, Health, and Society. He holds an MD and PhD in Immunology from Harvard.
David Cohan, MD, FACS
David is an oncology clinical development executive serving as VP of Global Clinical Development at Fortvita Biologics. He previously held roles at Pyxis Oncology and Replimune, where he contributed to the development of RP1 (vusolimogene oderparepvec), an oncolytic immunotherapy now under FDA priority review. He also held roles at Secura Bio and Alkermes. Before industry, he was an Attending Surgeon and Assistant Professor in Head & Neck Surgery at Roswell Park Comprehensive Cancer Center. He holds an MD from Stanford.
Chris Reist, MD
Psychiatry
Chris is a board-certified psychiatrist and Professor Emeritus at the University of California, Irvine. He has led over 40 clinical trials as principal investigator across PTSD, major depressive disorder, and schizophrenia, including novel approaches such as virtual reality exposure therapy and stellate ganglion blockade for PTSD. He has published over 80 papers on pharmacogenetics and psychiatric drug development, and previously served as Associate Chief of Staff for Research at the Long Beach VA Healthcare System, overseeing research infrastructure serving 40,000+ enrolled veterans.
Khawar Hussain
Dermatology
Khawar is a consultant dermatologist at Chelsea and Westminster Hospital NHS Foundation Trust, treating both paediatric and adult patients across atopic dermatitis, psoriasis, hidradenitis suppurativa, and acne. He is an Honorary Clinical Senior Lecturer at Imperial College London and a principal investigator on multiple active clinical research trials. He has published over 60 peer-reviewed papers, including research on checkpoint inhibitor-induced psoriasis and dupilumab outcomes in paediatric atopic dermatitis. He sits on national clinical guideline committees.

The people who run your trial understand how clinical complexity compounds. We built Lindus to stay ahead of it.

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