Date: Friday 19th November 2021 Time: 15:00-16:30 GMT Speakers: Paul Dorinsky (AstraZeneca) and David Wright (AstraZeneca)
Who is this event intended for? Clinicians, Regulators, Investigators, Academics, members of Ethics Committees, Statisticians, referees and editors of medical journals. What is the benefit of attending? Gain alignment on the clinical question(s) of interest; frame clinical questions which may be of interest to different stakeholders; be transparent when communicating trial results.
Overview
Building on the previous webinar series we will present a refresher on the key elements of the estimand framework and use the ETHOS study to illustrate the estimand framework and to highlight the different options that may be of interest to different stakeholders. The background and disease context of the case will be described, the important events (termed intercurrent events) occurring in the trial will be described and three estimands will be showcased. It will then be explored how best to communicate the estimands in medical journals.
Topics of discussion will be raised at different points during the training and there will be time allowed (30 mins) to answer your questions, which can be posted via the chat. Questions on how estimands should be communicated in medical journals and how to encourage their inclusion in journal articles are particularly encouraged.
To view the flyer for this webinar, please click here.
Registration
You can now register for this event. This event is free of charge to both Members and Non Members of PSI.
To register your place, please click here.
Speaker Details
Speaker
Biography
Paul Dorinsky
Dr. Paul Dorinsky has over 35 years of experience in Academic Medicine and Medicine Development and has more than 90 per-reviewed publications in Respiratory and Critical Care Medicine and Respiratory Medicine development. Dr. Dorinsky completed his undergraduate and medical training at the Ohio State University in Columbus, Ohio (USA). He received his undergraduate degree in mathematics in 1974 and his MD degree in 1978. He completed his Residency Training in Internal Medicine in 1981 and his Pulmonary and Critical Care Medicine training in 1983. He joined the Pulmonary and Critical Care Faculty of the Ohio State University in 1983 and remained in that position until 1998. He was director of the Medical Intensive care unit and published extensively on the subjects of sepsis, ARDS and multiple organ failure. He served as President of the Ohio Thoracic Society for 2 years. He also served as chairman of the Critical Care Assembly of the American Thoracic Society and was on the Board of American Thoracic Society for 2 years. He received funding from the American Lung Association, the American Heart Association and the NIH. He was also awarded an Edward Livingston Trudeau Fellowship award from the American Lung Association. Dr. Dorinsky has been involved in Respiratory clinical development for over 20 years. He joined Pearl/AstraZeneca in 2016 and led the clinical development program for Breztri and is currently the Global Clinical Head of the Aerosphere franchise.
David Wright
David Wright has been Head of Statistical Innovation at AstraZeneca since 2016 where he leads a group of experts in trial design and analysis of late phase clinical trials. Dr Wright received his BSc in Mathematics from the University of Leicester in 1989 and an MSc in Medical Statistics also from the University of Leicester in 1990. In 1995 Dr Wright received a PhD in Statistics from Queen Mary and Westfield College, University of London. From 1994 to 1996 Dr Wright did a Post Doc at the University of Warwick and he was a Lecturer in Medical Statistics at University College London from 1996 to 1999. From 1999 to 2016 Dr Wright worked at the Medicines and Healthcare products Regulatory Agency (MHRA (formerly the Medicines Control Agency (MCA) initially as a Statistical Assessor. From 2011 Dr Wright was an Expert Assessor and Deputy Unit Manager of the Statistics and Pharmacokinetics Unit. From 2011 to 2016 Dr Wright was the Chair of the Biostatistics Working Party (BSWP) at the European Medicines Agency (EMA). Dr Wright took the lead in revising the CHMP guideline on Missing Data in Confirmatory Clinical Trials in 2011 and is currently focused on the recent developments in the field of Estimands and the ramifications of the Addendum to ICH E9 on Estimands.
Scientific Meetings
PSI EIWG Webinar: Estimands from trial planning to publication in medical journals: The ETHOS trial
Date: Friday 19th November 2021 Time: 15:00-16:30 GMT Speakers: Paul Dorinsky (AstraZeneca) and David Wright (AstraZeneca)
Who is this event intended for? Clinicians, Regulators, Investigators, Academics, members of Ethics Committees, Statisticians, referees and editors of medical journals. What is the benefit of attending? Gain alignment on the clinical question(s) of interest; frame clinical questions which may be of interest to different stakeholders; be transparent when communicating trial results.
Overview
Building on the previous webinar series we will present a refresher on the key elements of the estimand framework and use the ETHOS study to illustrate the estimand framework and to highlight the different options that may be of interest to different stakeholders. The background and disease context of the case will be described, the important events (termed intercurrent events) occurring in the trial will be described and three estimands will be showcased. It will then be explored how best to communicate the estimands in medical journals.
Topics of discussion will be raised at different points during the training and there will be time allowed (30 mins) to answer your questions, which can be posted via the chat. Questions on how estimands should be communicated in medical journals and how to encourage their inclusion in journal articles are particularly encouraged.
To view the flyer for this webinar, please click here.
Registration
You can now register for this event. This event is free of charge to both Members and Non Members of PSI.
To register your place, please click here.
Speaker Details
Speaker
Biography
Paul Dorinsky
Dr. Paul Dorinsky has over 35 years of experience in Academic Medicine and Medicine Development and has more than 90 per-reviewed publications in Respiratory and Critical Care Medicine and Respiratory Medicine development. Dr. Dorinsky completed his undergraduate and medical training at the Ohio State University in Columbus, Ohio (USA). He received his undergraduate degree in mathematics in 1974 and his MD degree in 1978. He completed his Residency Training in Internal Medicine in 1981 and his Pulmonary and Critical Care Medicine training in 1983. He joined the Pulmonary and Critical Care Faculty of the Ohio State University in 1983 and remained in that position until 1998. He was director of the Medical Intensive care unit and published extensively on the subjects of sepsis, ARDS and multiple organ failure. He served as President of the Ohio Thoracic Society for 2 years. He also served as chairman of the Critical Care Assembly of the American Thoracic Society and was on the Board of American Thoracic Society for 2 years. He received funding from the American Lung Association, the American Heart Association and the NIH. He was also awarded an Edward Livingston Trudeau Fellowship award from the American Lung Association. Dr. Dorinsky has been involved in Respiratory clinical development for over 20 years. He joined Pearl/AstraZeneca in 2016 and led the clinical development program for Breztri and is currently the Global Clinical Head of the Aerosphere franchise.
David Wright
David Wright has been Head of Statistical Innovation at AstraZeneca since 2016 where he leads a group of experts in trial design and analysis of late phase clinical trials. Dr Wright received his BSc in Mathematics from the University of Leicester in 1989 and an MSc in Medical Statistics also from the University of Leicester in 1990. In 1995 Dr Wright received a PhD in Statistics from Queen Mary and Westfield College, University of London. From 1994 to 1996 Dr Wright did a Post Doc at the University of Warwick and he was a Lecturer in Medical Statistics at University College London from 1996 to 1999. From 1999 to 2016 Dr Wright worked at the Medicines and Healthcare products Regulatory Agency (MHRA (formerly the Medicines Control Agency (MCA) initially as a Statistical Assessor. From 2011 Dr Wright was an Expert Assessor and Deputy Unit Manager of the Statistics and Pharmacokinetics Unit. From 2011 to 2016 Dr Wright was the Chair of the Biostatistics Working Party (BSWP) at the European Medicines Agency (EMA). Dr Wright took the lead in revising the CHMP guideline on Missing Data in Confirmatory Clinical Trials in 2011 and is currently focused on the recent developments in the field of Estimands and the ramifications of the Addendum to ICH E9 on Estimands.
Training Courses
PSI EIWG Webinar: Estimands from trial planning to publication in medical journals: The ETHOS trial
Date: Friday 19th November 2021 Time: 15:00-16:30 GMT Speakers: Paul Dorinsky (AstraZeneca) and David Wright (AstraZeneca)
Who is this event intended for? Clinicians, Regulators, Investigators, Academics, members of Ethics Committees, Statisticians, referees and editors of medical journals. What is the benefit of attending? Gain alignment on the clinical question(s) of interest; frame clinical questions which may be of interest to different stakeholders; be transparent when communicating trial results.
Overview
Building on the previous webinar series we will present a refresher on the key elements of the estimand framework and use the ETHOS study to illustrate the estimand framework and to highlight the different options that may be of interest to different stakeholders. The background and disease context of the case will be described, the important events (termed intercurrent events) occurring in the trial will be described and three estimands will be showcased. It will then be explored how best to communicate the estimands in medical journals.
Topics of discussion will be raised at different points during the training and there will be time allowed (30 mins) to answer your questions, which can be posted via the chat. Questions on how estimands should be communicated in medical journals and how to encourage their inclusion in journal articles are particularly encouraged.
To view the flyer for this webinar, please click here.
Registration
You can now register for this event. This event is free of charge to both Members and Non Members of PSI.
To register your place, please click here.
Speaker Details
Speaker
Biography
Paul Dorinsky
Dr. Paul Dorinsky has over 35 years of experience in Academic Medicine and Medicine Development and has more than 90 per-reviewed publications in Respiratory and Critical Care Medicine and Respiratory Medicine development. Dr. Dorinsky completed his undergraduate and medical training at the Ohio State University in Columbus, Ohio (USA). He received his undergraduate degree in mathematics in 1974 and his MD degree in 1978. He completed his Residency Training in Internal Medicine in 1981 and his Pulmonary and Critical Care Medicine training in 1983. He joined the Pulmonary and Critical Care Faculty of the Ohio State University in 1983 and remained in that position until 1998. He was director of the Medical Intensive care unit and published extensively on the subjects of sepsis, ARDS and multiple organ failure. He served as President of the Ohio Thoracic Society for 2 years. He also served as chairman of the Critical Care Assembly of the American Thoracic Society and was on the Board of American Thoracic Society for 2 years. He received funding from the American Lung Association, the American Heart Association and the NIH. He was also awarded an Edward Livingston Trudeau Fellowship award from the American Lung Association. Dr. Dorinsky has been involved in Respiratory clinical development for over 20 years. He joined Pearl/AstraZeneca in 2016 and led the clinical development program for Breztri and is currently the Global Clinical Head of the Aerosphere franchise.
David Wright
David Wright has been Head of Statistical Innovation at AstraZeneca since 2016 where he leads a group of experts in trial design and analysis of late phase clinical trials. Dr Wright received his BSc in Mathematics from the University of Leicester in 1989 and an MSc in Medical Statistics also from the University of Leicester in 1990. In 1995 Dr Wright received a PhD in Statistics from Queen Mary and Westfield College, University of London. From 1994 to 1996 Dr Wright did a Post Doc at the University of Warwick and he was a Lecturer in Medical Statistics at University College London from 1996 to 1999. From 1999 to 2016 Dr Wright worked at the Medicines and Healthcare products Regulatory Agency (MHRA (formerly the Medicines Control Agency (MCA) initially as a Statistical Assessor. From 2011 Dr Wright was an Expert Assessor and Deputy Unit Manager of the Statistics and Pharmacokinetics Unit. From 2011 to 2016 Dr Wright was the Chair of the Biostatistics Working Party (BSWP) at the European Medicines Agency (EMA). Dr Wright took the lead in revising the CHMP guideline on Missing Data in Confirmatory Clinical Trials in 2011 and is currently focused on the recent developments in the field of Estimands and the ramifications of the Addendum to ICH E9 on Estimands.
Journal Club
PSI EIWG Webinar: Estimands from trial planning to publication in medical journals: The ETHOS trial
Date: Friday 19th November 2021 Time: 15:00-16:30 GMT Speakers: Paul Dorinsky (AstraZeneca) and David Wright (AstraZeneca)
Who is this event intended for? Clinicians, Regulators, Investigators, Academics, members of Ethics Committees, Statisticians, referees and editors of medical journals. What is the benefit of attending? Gain alignment on the clinical question(s) of interest; frame clinical questions which may be of interest to different stakeholders; be transparent when communicating trial results.
Overview
Building on the previous webinar series we will present a refresher on the key elements of the estimand framework and use the ETHOS study to illustrate the estimand framework and to highlight the different options that may be of interest to different stakeholders. The background and disease context of the case will be described, the important events (termed intercurrent events) occurring in the trial will be described and three estimands will be showcased. It will then be explored how best to communicate the estimands in medical journals.
Topics of discussion will be raised at different points during the training and there will be time allowed (30 mins) to answer your questions, which can be posted via the chat. Questions on how estimands should be communicated in medical journals and how to encourage their inclusion in journal articles are particularly encouraged.
To view the flyer for this webinar, please click here.
Registration
You can now register for this event. This event is free of charge to both Members and Non Members of PSI.
To register your place, please click here.
Speaker Details
Speaker
Biography
Paul Dorinsky
Dr. Paul Dorinsky has over 35 years of experience in Academic Medicine and Medicine Development and has more than 90 per-reviewed publications in Respiratory and Critical Care Medicine and Respiratory Medicine development. Dr. Dorinsky completed his undergraduate and medical training at the Ohio State University in Columbus, Ohio (USA). He received his undergraduate degree in mathematics in 1974 and his MD degree in 1978. He completed his Residency Training in Internal Medicine in 1981 and his Pulmonary and Critical Care Medicine training in 1983. He joined the Pulmonary and Critical Care Faculty of the Ohio State University in 1983 and remained in that position until 1998. He was director of the Medical Intensive care unit and published extensively on the subjects of sepsis, ARDS and multiple organ failure. He served as President of the Ohio Thoracic Society for 2 years. He also served as chairman of the Critical Care Assembly of the American Thoracic Society and was on the Board of American Thoracic Society for 2 years. He received funding from the American Lung Association, the American Heart Association and the NIH. He was also awarded an Edward Livingston Trudeau Fellowship award from the American Lung Association. Dr. Dorinsky has been involved in Respiratory clinical development for over 20 years. He joined Pearl/AstraZeneca in 2016 and led the clinical development program for Breztri and is currently the Global Clinical Head of the Aerosphere franchise.
David Wright
David Wright has been Head of Statistical Innovation at AstraZeneca since 2016 where he leads a group of experts in trial design and analysis of late phase clinical trials. Dr Wright received his BSc in Mathematics from the University of Leicester in 1989 and an MSc in Medical Statistics also from the University of Leicester in 1990. In 1995 Dr Wright received a PhD in Statistics from Queen Mary and Westfield College, University of London. From 1994 to 1996 Dr Wright did a Post Doc at the University of Warwick and he was a Lecturer in Medical Statistics at University College London from 1996 to 1999. From 1999 to 2016 Dr Wright worked at the Medicines and Healthcare products Regulatory Agency (MHRA (formerly the Medicines Control Agency (MCA) initially as a Statistical Assessor. From 2011 Dr Wright was an Expert Assessor and Deputy Unit Manager of the Statistics and Pharmacokinetics Unit. From 2011 to 2016 Dr Wright was the Chair of the Biostatistics Working Party (BSWP) at the European Medicines Agency (EMA). Dr Wright took the lead in revising the CHMP guideline on Missing Data in Confirmatory Clinical Trials in 2011 and is currently focused on the recent developments in the field of Estimands and the ramifications of the Addendum to ICH E9 on Estimands.
Webinars
PSI EIWG Webinar: Estimands from trial planning to publication in medical journals: The ETHOS trial
Date: Friday 19th November 2021 Time: 15:00-16:30 GMT Speakers: Paul Dorinsky (AstraZeneca) and David Wright (AstraZeneca)
Who is this event intended for? Clinicians, Regulators, Investigators, Academics, members of Ethics Committees, Statisticians, referees and editors of medical journals. What is the benefit of attending? Gain alignment on the clinical question(s) of interest; frame clinical questions which may be of interest to different stakeholders; be transparent when communicating trial results.
Overview
Building on the previous webinar series we will present a refresher on the key elements of the estimand framework and use the ETHOS study to illustrate the estimand framework and to highlight the different options that may be of interest to different stakeholders. The background and disease context of the case will be described, the important events (termed intercurrent events) occurring in the trial will be described and three estimands will be showcased. It will then be explored how best to communicate the estimands in medical journals.
Topics of discussion will be raised at different points during the training and there will be time allowed (30 mins) to answer your questions, which can be posted via the chat. Questions on how estimands should be communicated in medical journals and how to encourage their inclusion in journal articles are particularly encouraged.
To view the flyer for this webinar, please click here.
Registration
You can now register for this event. This event is free of charge to both Members and Non Members of PSI.
To register your place, please click here.
Speaker Details
Speaker
Biography
Paul Dorinsky
Dr. Paul Dorinsky has over 35 years of experience in Academic Medicine and Medicine Development and has more than 90 per-reviewed publications in Respiratory and Critical Care Medicine and Respiratory Medicine development. Dr. Dorinsky completed his undergraduate and medical training at the Ohio State University in Columbus, Ohio (USA). He received his undergraduate degree in mathematics in 1974 and his MD degree in 1978. He completed his Residency Training in Internal Medicine in 1981 and his Pulmonary and Critical Care Medicine training in 1983. He joined the Pulmonary and Critical Care Faculty of the Ohio State University in 1983 and remained in that position until 1998. He was director of the Medical Intensive care unit and published extensively on the subjects of sepsis, ARDS and multiple organ failure. He served as President of the Ohio Thoracic Society for 2 years. He also served as chairman of the Critical Care Assembly of the American Thoracic Society and was on the Board of American Thoracic Society for 2 years. He received funding from the American Lung Association, the American Heart Association and the NIH. He was also awarded an Edward Livingston Trudeau Fellowship award from the American Lung Association. Dr. Dorinsky has been involved in Respiratory clinical development for over 20 years. He joined Pearl/AstraZeneca in 2016 and led the clinical development program for Breztri and is currently the Global Clinical Head of the Aerosphere franchise.
David Wright
David Wright has been Head of Statistical Innovation at AstraZeneca since 2016 where he leads a group of experts in trial design and analysis of late phase clinical trials. Dr Wright received his BSc in Mathematics from the University of Leicester in 1989 and an MSc in Medical Statistics also from the University of Leicester in 1990. In 1995 Dr Wright received a PhD in Statistics from Queen Mary and Westfield College, University of London. From 1994 to 1996 Dr Wright did a Post Doc at the University of Warwick and he was a Lecturer in Medical Statistics at University College London from 1996 to 1999. From 1999 to 2016 Dr Wright worked at the Medicines and Healthcare products Regulatory Agency (MHRA (formerly the Medicines Control Agency (MCA) initially as a Statistical Assessor. From 2011 Dr Wright was an Expert Assessor and Deputy Unit Manager of the Statistics and Pharmacokinetics Unit. From 2011 to 2016 Dr Wright was the Chair of the Biostatistics Working Party (BSWP) at the European Medicines Agency (EMA). Dr Wright took the lead in revising the CHMP guideline on Missing Data in Confirmatory Clinical Trials in 2011 and is currently focused on the recent developments in the field of Estimands and the ramifications of the Addendum to ICH E9 on Estimands.
Careers Meetings
PSI EIWG Webinar: Estimands from trial planning to publication in medical journals: The ETHOS trial
Date: Friday 19th November 2021 Time: 15:00-16:30 GMT Speakers: Paul Dorinsky (AstraZeneca) and David Wright (AstraZeneca)
Who is this event intended for? Clinicians, Regulators, Investigators, Academics, members of Ethics Committees, Statisticians, referees and editors of medical journals. What is the benefit of attending? Gain alignment on the clinical question(s) of interest; frame clinical questions which may be of interest to different stakeholders; be transparent when communicating trial results.
Overview
Building on the previous webinar series we will present a refresher on the key elements of the estimand framework and use the ETHOS study to illustrate the estimand framework and to highlight the different options that may be of interest to different stakeholders. The background and disease context of the case will be described, the important events (termed intercurrent events) occurring in the trial will be described and three estimands will be showcased. It will then be explored how best to communicate the estimands in medical journals.
Topics of discussion will be raised at different points during the training and there will be time allowed (30 mins) to answer your questions, which can be posted via the chat. Questions on how estimands should be communicated in medical journals and how to encourage their inclusion in journal articles are particularly encouraged.
To view the flyer for this webinar, please click here.
Registration
You can now register for this event. This event is free of charge to both Members and Non Members of PSI.
To register your place, please click here.
Speaker Details
Speaker
Biography
Paul Dorinsky
Dr. Paul Dorinsky has over 35 years of experience in Academic Medicine and Medicine Development and has more than 90 per-reviewed publications in Respiratory and Critical Care Medicine and Respiratory Medicine development. Dr. Dorinsky completed his undergraduate and medical training at the Ohio State University in Columbus, Ohio (USA). He received his undergraduate degree in mathematics in 1974 and his MD degree in 1978. He completed his Residency Training in Internal Medicine in 1981 and his Pulmonary and Critical Care Medicine training in 1983. He joined the Pulmonary and Critical Care Faculty of the Ohio State University in 1983 and remained in that position until 1998. He was director of the Medical Intensive care unit and published extensively on the subjects of sepsis, ARDS and multiple organ failure. He served as President of the Ohio Thoracic Society for 2 years. He also served as chairman of the Critical Care Assembly of the American Thoracic Society and was on the Board of American Thoracic Society for 2 years. He received funding from the American Lung Association, the American Heart Association and the NIH. He was also awarded an Edward Livingston Trudeau Fellowship award from the American Lung Association. Dr. Dorinsky has been involved in Respiratory clinical development for over 20 years. He joined Pearl/AstraZeneca in 2016 and led the clinical development program for Breztri and is currently the Global Clinical Head of the Aerosphere franchise.
David Wright
David Wright has been Head of Statistical Innovation at AstraZeneca since 2016 where he leads a group of experts in trial design and analysis of late phase clinical trials. Dr Wright received his BSc in Mathematics from the University of Leicester in 1989 and an MSc in Medical Statistics also from the University of Leicester in 1990. In 1995 Dr Wright received a PhD in Statistics from Queen Mary and Westfield College, University of London. From 1994 to 1996 Dr Wright did a Post Doc at the University of Warwick and he was a Lecturer in Medical Statistics at University College London from 1996 to 1999. From 1999 to 2016 Dr Wright worked at the Medicines and Healthcare products Regulatory Agency (MHRA (formerly the Medicines Control Agency (MCA) initially as a Statistical Assessor. From 2011 Dr Wright was an Expert Assessor and Deputy Unit Manager of the Statistics and Pharmacokinetics Unit. From 2011 to 2016 Dr Wright was the Chair of the Biostatistics Working Party (BSWP) at the European Medicines Agency (EMA). Dr Wright took the lead in revising the CHMP guideline on Missing Data in Confirmatory Clinical Trials in 2011 and is currently focused on the recent developments in the field of Estimands and the ramifications of the Addendum to ICH E9 on Estimands.
Upcoming Events
Joint PSI/EFSPI Visualisation SIG 'Wonderful Wednesday' Webinars
Our monthly webinar explores examples of innovative data visualisations relevant to our day to day work. Each month a new dataset is provided from a clinical trial or other relevant example, and participants are invited to submit a graphic that communicates interesting and relevant characteristics of the data.
PSI Book Club - The Art of Explanation: How to Communicate with Clarity and Confidence
Develop your non-technical skills by reading The Art of Explanation by Ros Atkins and joining the Sept-Dec 2025 book club. You will be invited to join facilitated discussions of the concepts and ideas and apply skills from the book in-between sessions.
Our monthly webinar will allow attendees to gain practical knowledge and skills in Open-Source coding and tools, with a focus on applications in the pharmaceutical industry. The sessions will provide starting points in a number of areas, correct any common misconceptions and provide valuable resources for further learning.
This course is aimed at biostatisticians with no or some pediatric drug development experience who are interested to further their understanding. We will give you an introduction to the pediatric drug development landscape. This will include identifying the key regulations and processes governing pediatric development, a discussion on the needs and challenges when conducting pediatric research and a focus on the ways to overcome these challenges from a statistical perspective.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
Pre-Clinical SIG Webinar: AI agents for drug discovery and development
AI agents are large language models equipped with tools that can autonomously tackle challenging tasks. This talk will explore how generative AI agents can enable biomedical discovery.
EFSPI/PSI Causal Inference SIG Webinar: Instrumental Variable Methods
The webinar is targeted at statisticians working in the pharmaceutical industry, and the objective is to 1) provide a basic understanding of IV methodology including how it relates to causal inference, and 2) present two inspirational pharma-relevant applications.
The morning will be dedicated to networking opportunities, helping attendees build connections with peers and professionals. In the afternoon, participants can attend a series of talks and/or workshops, including a career panel featuring speakers from both academia and industry, offering insights into various career paths. There will also be a statistical workshop and a potential poster session. To wrap up the day, we’re exploring interest in an informal after-work networking event for those keen to continue the conversation.
The Pre-Clinical Special Interest Group (SIG) Workshop 2025 will take place over two half-days on 7 - 8 October in Verona, Italy, bringing together experts from industry, academia, and regulatory institutions to discuss key challenges and innovations in pre-clinical research.
PSI Training Course: Introduction to Machine Learning
Four sessions will include ML foundation (including an introduction, data exploration for ML and dimensionality reduction and feature selection), Supervised learning (including support vector machines and model evaluation and interpretation), model optimization and unsupervised learning (including clustering) and advanced topics (including neural networks, deep learning and large language models).
Webinar dedicated to the topic of stability modelling; opportunity to hear from statisticians working in the CMC field, with open question and answers. Brought to you by the CMC Statistical Network Europe (CSNE) SIG.
The program will feature insightful sessions led by distinguished invited speakers, alongside a poster session showcasing the latest advancements in the field. Further details will be provided.
Date: 19 November 2025
This event is aimed at students with an interest in the field of Medical Statistics, for example within pharmaceuticals, healthcare and/or medical research.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
Associate Director Biostatistics in Early Development - Novartis
As an Associate Director Biostatistics Early Development, you will be a key member of our biostatistics group, you will play a crucial role in the design, analysis, and interpretation of clinical trials for early development programs.
Associate Director Biostatistics, Real World Data - Novartis
If you are passionate about biostatistics and real-world data, and are looking for an exciting opportunity to contribute to groundbreaking research, we encourage you to apply.
Are you passionate about making a difference in the world of healthcare? Novartis is seeking a dynamic and experienced professional to join our team in London at The Westworks.
Director of HTA Biostatistics & Medical Affairs - Novartis
As the Director of HTA Biostatistics & Medical Affairs, you will play a pivotal role in shaping the future of healthcare by providing strategic biostatistical leadership and expertise.
Senior Medical Statistician & Statistical Programmer
An exciting opportunity has arisen for a permanent Senior Medical Statistician & Statistical Programmer to join the UKCRC fully registered Derby Clinical Trials Support Unit (Derby CTSU).
As a Senior Principal Biostatistician, you will be responsible and accountable for all statistical work, both scientific and operational, for one or more assigned clinical trials
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