It’s been another remarkable year for global biopharma, and the Scrip team is delighted to reveal the companies, teams and individuals who have made the shortlist for the 22nd annual Scrip Awards.
Congratulations to everyone shortlisted you represent the very best of an industry that continues to innovate, take bold risks and, above all, improve patients’ lives around the world.
Made the shortlist? Here’s what happens next.
If you’ve been shortlisted, you qualify for a specially discounted table at the awards evening so you can celebrate alongside the leading names in pharma at the black-tie gala dinner and ceremony at Raffles London at the OWO on Wednesday, 2 December 2026, with headline sponsor ICON.
Whether you’re on the shortlist or simply want to be part of a night that celebrates excellence across the global biopharma landscape, we’d love to see you there. To book your seat or table, or if you have any questions about the ceremony, reach out to the Scrip Awards team at natalia.kay@citeline.com.
Wednesday, 2 December 2026
Drinks reception from 6.30pm
Raffles London at the OWO
Drinks reception from 6.30pm
Sponsorship available
Category & bespoke packages
Enquire about sponsorship →
Click here to see our full entry guide for more information.
For any enquiries about the Scrip Awards 2026, please contact us at natalia.kay@citeline.com.
The Best New Drug Award recognizes excellence in pharmaceutical development. Launching innovative new products is the most important function of the industry, and a successful new drug launch marks the culmination of years of risky and expensive R&D. In this category, the judges will be looking for the small-molecule or biological product that was approved in its first market worldwide during the qualifying period that represents the best therapeutic advance in its area.
FINALISTS
This Award seeks to recognize success in a clinical trial of a new drug product (biological or chemical) that is expected to lead to an advance in healthcare. This might include the first demonstration of a clear clinical effect for a new drug in an area of unmet medical need, a pivotal study of a new drug with a breakthrough mechanism of action, or a major study of a potential new or expanded indication for an already marketed product. The product involved need not yet be approved, but the judges will be looking for innovation, clear proof of benefit and potential commercial reward. To be eligible, the study in question must have been presented for peer review at a major medical meeting or been published in a scientific journal between 1 July 2025 – 30 June 2026.
FINALISTS
FINALISTS
Deals are vital both in helping to keep pharma’s pipelines replenished and in generating income for smaller firms or exits for investors. Deals considered here are those that involve the licensing of a particular drug, project or group of closely related drugs/projects from one company to another for further development and/or marketing, or M&A deals centred around a product or group of related products. Please note, it does not include more involved partnerships between companies to explore particular therapeutic strategies (see Criteria for the Best Partnership Alliance)
FINALISTS
Scrip’s Best Partnership Alliance Award recognizes the importance of pharmaceutical and/or biotech companies working together to develop new medicines from the earliest stages. This category seeks to reward innovative partnerships between companies in which they share the risks and rewards inherent in exploring novel therapeutic strategies and developing new drugs.
FINALISTS
The biotech industry’s entrepreneurial spirit and cutting-edge science have transformed the research and development of medicines in the past few decades. This Award honours outstanding achievement by biotech companies over the qualifying 12 months.
FINALISTS
The Awards for the Best Contract Research Organization acknowledge the critical role that CROs play in drug development. Clinical outsourcing is vital as the pharmaceutical industry seeks to benefit more and more from these specialist companies’ experience in handling all aspects of clinical trials. The Awards for CROs are split into two sister categories to separate the larger full-service providers from those smaller CROs that provide specialist services to their clients.
FINALISTS
The Awards for the Best Contract Research Organization acknowledge the critical role that CROs play in drug development. Clinical outsourcing is vital as the pharmaceutical industry seeks to benefit more and more from these specialist companies’ experience in handling all aspects of clinical trials. The Awards for CROs are split into two sister categories to separate the larger full-service providers from those smaller CROs that provide specialist services to their clients.
FINALISTS
This new Scrip Award seeks to recognize early clinical advances in oncology made by small biopharma companies. The great strides seen in cancer therapies in recent years often had their genesis in the labs of specialist firms. We are looking to reward companies that are exploiting new knowledge in cancer cell biology and the tumor microenvironment to forge new paths to tackle the disease, for instance by developing novel therapeutic strategies in immuno-oncology, gene and cell therapies and new targeted agents.
This category is aimed at clinical-stage oncology firms pioneering new approaches in the treatment of cancer that have shown proof of concept in early (Phase I or II) clinical trials and have candidates moving forward in the development pathway.
FINALISTS
Scrip’s Business Development Team of the Year Award will honor the achievements of business development teams whether they are from a pharma or biotech company or a cross-company team responsible for a specific deal or collaborative project which took place between 1 July 2025 – 30 June 2026.
FINALISTS
This Award is designed to acknowledge the numerous ways in which pharma and biotech companies give back to the wider community. This could include outreach within a local community, with a charity or patient advocacy group, or alongside an NGO or humanitarian organization.
FINALISTS
This new category seeks to reward AI innovation in tasks such as improving clinical trial design, site selection and recruitment, identifying responders, reducing protocol burden and improving operational performance.
FINALISTS
This new category seeks to reward AI innovation in tasks such as identifying targets, validating biology, discovering candidates, optimizing molecules and improving preclinical decision making.
FINALISTS
The Pharma Company of the Year Award honors outstanding achievements by pharmaceutical companies over the qualifying 12 months between 1 July 2025 – 30 June 2026.
This special Award is chosen by Scrip’s senior editorial team, based on a variety of key metrics. The winner will be announced on the night of the Scrip Awards.
The winner of this Award will be an exceptional individual with a consistent history of service, above and beyond the call of duty, throughout their career. This prestigious international Award will go to someone who has had a distinguished career in the biotech or pharmaceutical arena, primarily within industry.
ICON plc is a world-leading clinical research organisation. Offering deep operational and medical expertise we accelerate innovation, driving emerging therapies forward to improve patient outcomes. From molecule to medicine, we deliver integrated consulting, clinical development, commercialisation and post-marketing solutions to pharmaceutical, biotechnology, medical device, government and public health organisations worldwide.
Our focus is on addressing the full spectrum of clinical development challenges, not just point-of-service delivery. An extensive services portfolio and technology capabilities, combined with flexible delivery and models, allow us to reduce development time and costs for clients.
For further information about ICON, visit: www.iconplc.com.
Two-thirds of life science assets never realize their full value, and most fall short for commercial reasons rather than scientific ones. Blue Matter exists to close that gap.
Blue Matter is a global consulting firm dedicated exclusively to the life sciences: 450+ specialists helping biopharma companies unlock the full potential of their scientific innovations, from insight to action. The firm has supported more than 400 clients, including 18 of the top 20 global biopharma companies and hundreds of emerging, development-stage, and mid-size innovators. Its capabilities span primary research and analytics, strategic and operational consulting, implementation support, and communications, with true practitioner depth across R&D, Business Development, Market Access, Medical Affairs, Marketing and Communications, Sales, and Supply Chain. Blue Matter integrates that expertise into teams built around each client's medical, market access, and commercial objectives.
Senior experts lead every engagement, and clients stay: repeat business exceeds 90%.
eClinical Solutions brings people & data together to support tomorrow's breakthroughs with clinical data software and clinical biometrics services.
Parexel is a leading global clinical development partner providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our 22,000+ global employees work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart™. We continue to earn recognition industrywide, including the 2025 Scrip Award for “Best Contract Research Organization – Full-Service Provider,” 2024 Fierce Biotech CRO Award for "Innovative Approaches to Patient-Centric Research" and the 2024 and 2023 Society for Clinical Research Sites (SCRS) Eagle Award for advancing the clinical research profession through strong site partnerships. For more information, visit parexel.com and follow us on LinkedIn, X, Facebook and Instagram.
Vaidheesh Annaswamy
Executive Chairman
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Executive Chairman
Suven Pharma
Vaidheesh Annaswamy is a successful senior business leader from the most admired Fortune 100 companies with more than 35 years of diverse experience in the healthcare and FMCG Industry, including at Johnson and Johnson, Pfizer and GSK. He has proven expertise in general management with a strong background in market creation and leadership development. Further, he has rich experience in building strong leadership for brands/franchises across varied categories (healthcare and FMCG) and in multi-grid and multi-cultural Locations in the Asia-Pacific region.
Vaidheesh Annaswamy is a successful senior business leader from the most admired Fortune 100 companies with more than 35 years of diverse experience in the healthcare and FMCG Industry, including at Johnson and Johnson, Pfizer and GSK. He has proven expertise in general management with a strong background in market creation and leadership development. Further, he has rich experience in building strong leadership for brands/franchises across varied categories (healthcare and FMCG) and in multi-grid and multi-cultural Locations in the Asia-Pacific region.
Jane Bentley
VP Oncology Therapeutic Strategy and Innovation
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VP Oncology Therapeutic Strategy and Innovation
Insitute of Clinical Research
Jane holds a BSc in Pharmacology and a PhD in Toxicology from the University of London and recently completed an MBA in International Health Care Management. As a board member at the Institute of Clinical Research, she helps shape its strategic direction and promote clinical research careers. With over 35 years of experience in oncology drug development, including executive leadership and project management, she now focuses on driving strategic innovation in oncology and collaborating with pharma and biotech companies to enhance drug development.
Jane holds a BSc in Pharmacology and a PhD in Toxicology from the University of London and recently completed an MBA in International Health Care Management. As a board member at the Institute of Clinical Research, she helps shape its strategic direction and promote clinical research careers. With over 35 years of experience in oncology drug development, including executive leadership and project management, she now focuses on driving strategic innovation in oncology and collaborating with pharma and biotech companies to enhance drug development.
Laura Brown
Pharmaceutical Training Consultant Course Director
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Pharmaceutical Training Consultant Course Director
University of Cardiff
Dr Laura Brown is Course Director of the MSc in Clinical Research, University of Cardiff and a Training and QA Consultant. Dr Brown has held a number of international and senior management positions in the pharmaceutical industry. She has worked for several international companies including GlaxoWellcome, Hoechst Marion Roussel and Phoenix International. She was a member of the Editorial board of the Good Clinical Practice Journal for 10 years. She is author of several books including Project Management for the Pharmaceutical Industry, a Practical Guide to the Clinical Trial Directive and several articles on the new EU Clinical Trial Regulation.
Dr Laura Brown is Course Director of the MSc in Clinical Research, University of Cardiff and a Training and QA Consultant. Dr Brown has held a number of international and senior management positions in the pharmaceutical industry. She has worked for several international companies including GlaxoWellcome, Hoechst Marion Roussel and Phoenix International. She was a member of the Editorial board of the Good Clinical Practice Journal for 10 years. She is author of several books including Project Management for the Pharmaceutical Industry, a Practical Guide to the Clinical Trial Directive and several articles on the new EU Clinical Trial Regulation.
Daniel Chancellor
VP of Thought Leadership
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VP of Thought Leadership
Norstella
Daniel has nearly 20 years of experience spanning drug development, market analysis, consulting and pharmaceutical strategy. This gives him a broad view of what is required to bring therapies to market and where important operational and strategic pain points occur. His focus is on applying AI where it creates genuine value rather than introducing additional technology or complexity.
What makes Norstella's AI different?
The differentiator is the breadth of the underlying pharmaceutical dataset. Norstella can connect information from across the pipeline-to-patient journey, creating insights that would be difficult to generate from isolated datasets. AI extends the value that can be derived from that information.
What can pharma teams do now that was not possible two years ago?
One major advance is the ability to understand how patients appear in real-world healthcare and translate this into more effective targeting. AI can help bridge the gap between the controlled environment of a clinical trial and the much less structured reality of patient treatment.
How can AI accelerate the journey from pipeline to patient?
Trial design, portfolio investment and market access decisions all consume substantial time. AI can help organisations make these decisions using a broader evidence base and do so more quickly, supporting faster development and potentially wider access to successful therapies.
Brian Hargreaves
Independent Advisor
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Independent Advisor
Former Pharma Exec and Biotech VC with 3i plc
His career in Healthcare spans academia, Pharma, Venture Capital and Private Equity. Following his early career as a Lecturer in Pharmacy at Manchester University, he had a series of commercial and international marketing roles with Smith Kline and French, Mundipharma, Wellcome, Glaxo Wellcome and with Astra Hässle where he led the commercialisation of the blockbuster product, Nexium. In 1997, he moved to 3i plc in the innovative growth period of biotech Venture Capital.
Trevor Jones
Director
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Director
E-Therapeutics
Jones is chairman of the Oxford-based AI drug discovery company e-Therapeutics and a member of the board of the USA vaccine company Techimmune LLC. He was formerly R&D Director of the Wellcome Foundation, a director of Allergan Inc. and Director General of the Association of the British pharmaceutical industry (ABPI ). He is a visiting professor at Kings College London.
Jones is chairman of the Oxford-based AI drug discovery company e-Therapeutics and a member of the board of the USA vaccine company Techimmune LLC. He was formerly R&D Director of the Wellcome Foundation, a director of Allergan Inc. and Director General of the Association of the British pharmaceutical industry (ABPI ). He is a visiting professor at Kings College London.
Viren Mehta
Founder
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Founder
Mehta Partners
Viren is the founder and managing member of Mehta Partners, LLC, where his analytical insights on global healthcare have shaped biopharmaceutical strategies and investments. With over 30 years of experience and degrees from the University of Southern California and UCLA, he has worked closely with BioPharma leaders and investment managers. His recent initiative, Gather Health, aims to enhance patient outcomes by connecting patients with their healthcare providers and personal networks. Viren also contributes to philanthropy through the Viram Foundation and has a background in strategic planning with Merck & Co., Wood MacKenzie, and S.G. Warburg.
Viren is the founder and managing member of Mehta Partners, LLC, where his analytical insights on global healthcare have shaped biopharmaceutical strategies and investments. With over 30 years of experience and degrees from the University of Southern California and UCLA, he has worked closely with BioPharma leaders and investment managers. His recent initiative, Gather Health, aims to enhance patient outcomes by connecting patients with their healthcare providers and personal networks. Viren also contributes to philanthropy through the Viram Foundation and has a background in strategic planning with Merck & Co., Wood MacKenzie, and S.G. Warburg.
Phornvit Phacharintanakul
Chairman
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Chairman
Strategic Business Partners
His experience extends across sales and marketing as well as country management of an international life science corporation. His current focus is in competency development of people through education, both formal and informal. Phornvit also sits on committees of national bodies in education and business. His academic background is in economics and business administration.
His experience extends across sales and marketing as well as country management of an international life science corporation. His current focus is in competency development of people through education, both formal and informal. Phornvit also sits on committees of national bodies in education and business. His academic background is in economics and business administration.
Peter Pitts
President
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President
Center for Medicine in the Public Interest
Peter Pitts is a Visiting Professor at the University of Paris Medical School and President of the Center for Medicine in the Public Interest. He previously served as an Associate Commissioner of the US FDA and is active with the Council for International Organizations of Medical Sciences (CIOMS) to enhance patient involvement in medicine development. Pitts has authored numerous publications in top journals like The Lancet and Nature Biotechnology, and holds editorial roles with various medical and regulatory science publications. He is based in New York City.
Peter Pitts is a Visiting Professor at the University of Paris Medical School and President of the Center for Medicine in the Public Interest. He previously served as an Associate Commissioner of the US FDA and is active with the Council for International Organizations of Medical Sciences (CIOMS) to enhance patient involvement in medicine development. Pitts has authored numerous publications in top journals like The Lancet and Nature Biotechnology, and holds editorial roles with various medical and regulatory science publications. He is based in New York City.
Andy Smith
Life Science Analyst
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Life Science Analyst
Equity Development
Smith began his career in research and development with ICI and SmithKline Beecham, and later transitioned to commercial roles at SB Pharmaceuticals, focusing on global brand management. After earning a PhD in Molecular Biology and an MBA, he moved into asset management and venture capital with 3i Group, managing several life science funds and winning the Techmark technology fund manager of the year award in 2007. He subsequently worked as director of business development and head of corporate finance at PharmaVentures, and taught life science valuation at the University of Cambridge. In 2017, Smith joined ICON's Pricing & Market Access group, advising on product valuation and commercialization, and later returned to work at Edison.
Smith began his career in research and development with ICI and SmithKline Beecham, and later transitioned to commercial roles at SB Pharmaceuticals, focusing on global brand management. After earning a PhD in Molecular Biology and an MBA, he moved into asset management and venture capital with 3i Group, managing several life science funds and winning the Techmark technology fund manager of the year award in 2007. He subsequently worked as director of business development and head of corporate finance at PharmaVentures, and taught life science valuation at the University of Cambridge. In 2017, Smith joined ICON's Pricing & Market Access group, advising on product valuation and commercialization, and later returned to work at Edison.
Robert Speigel
Founder
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Founder
Spiegel Consulting
Dr. Spiegel has over 30 years of extensive R&D and operational experience in biopharmaceuticals including Big Pharma, biotech, and academic startups as well as advisory roles with venture capital and private equity. Dr Spiegel was Director of the Developmental Therapeutics Program at NYU Medical Center and then spent over 25 years at Schering-Plough where he joined as the first Director for Oncology Clinical Research. He subsequently held a series of senior executive positions, including Senior Vice President for worldwide Clinical Research and Chief Medical Officer. During his time at Schering-Plough he took numerous drug candidates through clinical development and was involved with over 30 NDA approvals. Since 2011 Dr. Spiegel has been a consultant to the biotech industry and has served on the Scientific Advisory Board and Board of Directors of multiple biotech companies. He is currently the president of Spiegel Consulting LLC and an Assistant Professor of Medicine at Weill Cornell Medical College. He is also a Senior Advisor to the private equity firm Warburg Pincus and an Advisor to the Israel Biotech Fund. Dr. Spiegel received his B.A. from Yale University and his M.D. from the University of Pennsylvania. He completed his specialty training at the National Cancer Institute, National Institutes of Health (NIH).
Dr. Spiegel has over 30 years of extensive R&D and operational experience in biopharmaceuticals including Big Pharma, biotech, and academic startups as well as advisory roles with venture capital and private equity. Dr Spiegel was Director of the Developmental Therapeutics Program at NYU Medical Center and then spent over 25 years at Schering-Plough where he joined as the first Director for Oncology Clinical Research. He subsequently held a series of senior executive positions, including Senior Vice President for worldwide Clinical Research and Chief Medical Officer. During his time at Schering-Plough he took numerous drug candidates through clinical development and was involved with over 30 NDA approvals. Since 2011 Dr. Spiegel has been a consultant to the biotech industry and has served on the Scientific Advisory Board and Board of Directors of multiple biotech companies. He is currently the president of Spiegel Consulting LLC and an Assistant Professor of Medicine at Weill Cornell Medical College. He is also a Senior Advisor to the private equity firm Warburg Pincus and an Advisor to the Israel Biotech Fund. Dr. Spiegel received his B.A. from Yale University and his M.D. from the University of Pennsylvania. He completed his specialty training at the National Cancer Institute, National Institutes of Health (NIH).
Brian Tempest
Editor In Chief
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Editor In Chief
Journal of Generic Medicines
Dr Brian Tempest has held many Non-Executive roles in the Corporate, Educational and NGO Sectors. These positions include Pharmaceuticals, Hospital Management, Medical Diagnostics, Packaging, Financial Services, University Advisory Boards and the United Nations Patent Pool. He is currently Non-Executive Chairman of Touch Medical Media Group Holdings in the UK and is on the Board of a number of international Healthcare Companies as well as advising others from Europe and Asia.
Dr Brian Tempest has held many Non-Executive roles in the Corporate, Educational and NGO Sectors. These positions include Pharmaceuticals, Hospital Management, Medical Diagnostics, Packaging, Financial Services, University Advisory Boards and the United Nations Patent Pool. He is currently Non-Executive Chairman of Touch Medical Media Group Holdings in the UK and is on the Board of a number of international Healthcare Companies as well as advising others from Europe and Asia.
Brian has previously worked for GSK, Pfizer, Sanofi and Sun Pharmaceuticals in leadership positions. He holds FRSC, FRSM, BSc, PhD and DSc qualifications and now resides in Wales, UK.
Mike Ward
Award-Winning Writer, Editor, Commentator and Thought Leadership Leader
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Award-Winning Writer, Editor, Commentator and Thought Leadership Leader
Mike Ward is a highly regarded, award-winning writer, editor, commentator and thought leadership leader with more than four decades of experience covering the global life sciences and healthcare industries. Throughout his career, he has held senior editorial and content leadership positions at several of the industry's most influential organisations, including BioCentury, Informa and Clarivate.
Mike Ward is a highly regarded, award-winning writer, editor, commentator and thought leadership leader with more than four decades of experience covering the global life sciences and healthcare industries. Throughout his career, he has held senior editorial and content leadership positions at several of the industry's most influential organisations, including BioCentury, Informa and Clarivate.
Widely recognised for his ability to translate complex scientific, commercial and policy developments into compelling business intelligence, Mike has written extensively on drug discovery, clinical development, healthcare innovation, regulatory change and pharmaceutical strategy. He is a sought-after moderator, interviewer and speaker, having led discussions with industry executives, scientists, investors and policymakers across the global life sciences ecosystem.
Over the course of his career, Mike has built a reputation as one of the sector's most respected voices, combining deep industry knowledge with a talent for identifying emerging trends and helping organisations understand their strategic implications. His work has informed senior decision-makers across the pharmaceutical, biotechnology, investment and healthcare communities.