The PSI 2022 Conference took place at Gothia Towers, Gothenburg, Sweden from 12th to 15th June.
The conference consisted of a variety of plenary and parallel sessions, as well as breakout discussion sessions, workshops, a poster session and the Annual General Meeting. The conference ran over three full days from Monday to Wednesday, with a choice from two optional half day training course on the Sunday afternoon.
The 2022 Conference was a great success and was the highest attended PSI conference to date. Thank you to everyone involved; speakers, poster presenters, delegates, exhibitors, sponsors, MCI and the PSI scientific committee, for contributing to another successful conference.
David Lawrence, 2022 PSI Conference Chair
Kate Taylor, 2022 PSI Conference Vice-Chair
Paul Terrill, 2021 PSI Conference Vice-Chair
To access the recorded sessions from the PSI 2022 Conference, please visit our Video on Demand homepage.
To source the Conference content, simply select 'PSI 2022 Conference' from the 'Collection' dropdown menu. This will filter all available content to only show on-demand sessions from the 2022 Conference.
Please note: these are only available to view for Members of PSI, and will need to be signed in to watch them.
Some of this year's sessions are unfortunately not available to view on-demand, however we have made the slide decks available. Please see Session Titles listed below, with slide decks available to download beneath.
Please note: these are only accessible for Members of PSI, and will need to be signed in to access them.
Dealing with Non-Proportional Hazards
Everything better on average Calculating sample sizes based on average hazard ratio
Group-sequential stratified weighted log-rank tests in immuno-oncology
Estimands in Practice
Implementing Estimand Framework – Not So Simple!
Roche's estimand journey what we have learned and our future plans
Single World Intervention Graphs for Defining, Identifying, and Communicating Estimands in Clinical Trials
FMS (Swedish Society for Medical Statistics)
Selection bias and multiple inclusion criteria in observational studies
Statistical approaches and considerations when using an external control arm for a rare disease project
Travel vaccines strongly reduce mortality in cancer patients – a real effect or residual confounding
Master Protocols
Bayesian sample size planning for basket trials permitting borrowing of information
Phase II Basket Trials with Pruning and Pooling as Compared to Bayesian Hierarchical Models
Statistical catalysts Influencing an Externally Sponsored platform trial in COVID-19
Platform Trials
Designing an Adaptive Platform Trial in Tuberculosis
Drug combination development to treat infectious diseases Piranga platform trial case study
The EU-PEARL framework to design and conduct platform trials.
The TOGETHER Platform Trial - A multi-center, adaptive, randomized, platform trial to evaluate the effect of repurposed medicines in outpatient
PSI/RSS Prize-Winner's Session
Strategies for improving the assessment of probability of success (PoS) in late stage drug development
Using R for Regulatory Work
Using R for Regulatory Work (combined slides)
Historical Data SIG - framework part 1
Part 1 slides
Launch & Lifecycle SIG - are medical affairs the wild west of statistics
Are medical affairs the wild west of statistics (combined slides)
RWD SIG - Opportunities and Methodological Challenges
Alexander Schacht and Elizabeth Merrall's Slides
Deepak Parashar's slides
Intro slides
The PSI 2022 Conference took place at Gothia Towers, Gothenburg, Sweden from 12th to 15th June.
The conference consisted of a variety of plenary and parallel sessions, as well as breakout discussion sessions, workshops, a poster session and the Annual General Meeting. The conference ran over three full days from Monday to Wednesday, with a choice from two optional half day training course on the Sunday afternoon.
The 2022 Conference was a great success and was the highest attended PSI conference to date. Thank you to everyone involved; speakers, poster presenters, delegates, exhibitors, sponsors, MCI and the PSI scientific committee, for contributing to another successful conference.
David Lawrence, 2022 PSI Conference Chair
Kate Taylor, 2022 PSI Conference Vice-Chair
Paul Terrill, 2021 PSI Conference Vice-Chair
To access the recorded sessions from the PSI 2022 Conference, please visit our Video on Demand homepage.
To source the Conference content, simply select 'PSI 2022 Conference' from the 'Collection' dropdown menu. This will filter all available content to only show on-demand sessions from the 2022 Conference.
Please note: these are only available to view for Members of PSI, and will need to be signed in to watch them.
Some of this year's sessions are unfortunately not available to view on-demand, however we have made the slide decks available. Please see Session Titles listed below, with slide decks available to download beneath.
Please note: these are only accessible for Members of PSI, and will need to be signed in to access them.
Dealing with Non-Proportional Hazards
Everything better on average Calculating sample sizes based on average hazard ratio
Group-sequential stratified weighted log-rank tests in immuno-oncology
Estimands in Practice
Implementing Estimand Framework – Not So Simple!
Roche's estimand journey what we have learned and our future plans
Single World Intervention Graphs for Defining, Identifying, and Communicating Estimands in Clinical Trials
FMS (Swedish Society for Medical Statistics)
Selection bias and multiple inclusion criteria in observational studies
Statistical approaches and considerations when using an external control arm for a rare disease project
Travel vaccines strongly reduce mortality in cancer patients – a real effect or residual confounding
Master Protocols
Bayesian sample size planning for basket trials permitting borrowing of information
Phase II Basket Trials with Pruning and Pooling as Compared to Bayesian Hierarchical Models
Statistical catalysts Influencing an Externally Sponsored platform trial in COVID-19
Platform Trials
Designing an Adaptive Platform Trial in Tuberculosis
Drug combination development to treat infectious diseases Piranga platform trial case study
The EU-PEARL framework to design and conduct platform trials.
The TOGETHER Platform Trial - A multi-center, adaptive, randomized, platform trial to evaluate the effect of repurposed medicines in outpatient
PSI/RSS Prize-Winner's Session
Strategies for improving the assessment of probability of success (PoS) in late stage drug development
Using R for Regulatory Work
Using R for Regulatory Work (combined slides)
Historical Data SIG - framework part 1
Part 1 slides
Launch & Lifecycle SIG - are medical affairs the wild west of statistics
Are medical affairs the wild west of statistics (combined slides)
RWD SIG - Opportunities and Methodological Challenges
Alexander Schacht and Elizabeth Merrall's Slides
Deepak Parashar's slides
Intro slides
The PSI 2022 Conference took place at Gothia Towers, Gothenburg, Sweden from 12th to 15th June.
The conference consisted of a variety of plenary and parallel sessions, as well as breakout discussion sessions, workshops, a poster session and the Annual General Meeting. The conference ran over three full days from Monday to Wednesday, with a choice from two optional half day training course on the Sunday afternoon.
The 2022 Conference was a great success and was the highest attended PSI conference to date. Thank you to everyone involved; speakers, poster presenters, delegates, exhibitors, sponsors, MCI and the PSI scientific committee, for contributing to another successful conference.
David Lawrence, 2022 PSI Conference Chair
Kate Taylor, 2022 PSI Conference Vice-Chair
Paul Terrill, 2021 PSI Conference Vice-Chair
To access the recorded sessions from the PSI 2022 Conference, please visit our Video on Demand homepage.
To source the Conference content, simply select 'PSI 2022 Conference' from the 'Collection' dropdown menu. This will filter all available content to only show on-demand sessions from the 2022 Conference.
Please note: these are only available to view for Members of PSI, and will need to be signed in to watch them.
Some of this year's sessions are unfortunately not available to view on-demand, however we have made the slide decks available. Please see Session Titles listed below, with slide decks available to download beneath.
Please note: these are only accessible for Members of PSI, and will need to be signed in to access them.
Dealing with Non-Proportional Hazards
Everything better on average Calculating sample sizes based on average hazard ratio
Group-sequential stratified weighted log-rank tests in immuno-oncology
Estimands in Practice
Implementing Estimand Framework – Not So Simple!
Roche's estimand journey what we have learned and our future plans
Single World Intervention Graphs for Defining, Identifying, and Communicating Estimands in Clinical Trials
FMS (Swedish Society for Medical Statistics)
Selection bias and multiple inclusion criteria in observational studies
Statistical approaches and considerations when using an external control arm for a rare disease project
Travel vaccines strongly reduce mortality in cancer patients – a real effect or residual confounding
Master Protocols
Bayesian sample size planning for basket trials permitting borrowing of information
Phase II Basket Trials with Pruning and Pooling as Compared to Bayesian Hierarchical Models
Statistical catalysts Influencing an Externally Sponsored platform trial in COVID-19
Platform Trials
Designing an Adaptive Platform Trial in Tuberculosis
Drug combination development to treat infectious diseases Piranga platform trial case study
The EU-PEARL framework to design and conduct platform trials.
The TOGETHER Platform Trial - A multi-center, adaptive, randomized, platform trial to evaluate the effect of repurposed medicines in outpatient
PSI/RSS Prize-Winner's Session
Strategies for improving the assessment of probability of success (PoS) in late stage drug development
Using R for Regulatory Work
Using R for Regulatory Work (combined slides)
Historical Data SIG - framework part 1
Part 1 slides
Launch & Lifecycle SIG - are medical affairs the wild west of statistics
Are medical affairs the wild west of statistics (combined slides)
RWD SIG - Opportunities and Methodological Challenges
Alexander Schacht and Elizabeth Merrall's Slides
Deepak Parashar's slides
Intro slides
The PSI 2022 Conference took place at Gothia Towers, Gothenburg, Sweden from 12th to 15th June.
The conference consisted of a variety of plenary and parallel sessions, as well as breakout discussion sessions, workshops, a poster session and the Annual General Meeting. The conference ran over three full days from Monday to Wednesday, with a choice from two optional half day training course on the Sunday afternoon.
The 2022 Conference was a great success and was the highest attended PSI conference to date. Thank you to everyone involved; speakers, poster presenters, delegates, exhibitors, sponsors, MCI and the PSI scientific committee, for contributing to another successful conference.
David Lawrence, 2022 PSI Conference Chair
Kate Taylor, 2022 PSI Conference Vice-Chair
Paul Terrill, 2021 PSI Conference Vice-Chair
To access the recorded sessions from the PSI 2022 Conference, please visit our Video on Demand homepage.
To source the Conference content, simply select 'PSI 2022 Conference' from the 'Collection' dropdown menu. This will filter all available content to only show on-demand sessions from the 2022 Conference.
Please note: these are only available to view for Members of PSI, and will need to be signed in to watch them.
Some of this year's sessions are unfortunately not available to view on-demand, however we have made the slide decks available. Please see Session Titles listed below, with slide decks available to download beneath.
Please note: these are only accessible for Members of PSI, and will need to be signed in to access them.
Dealing with Non-Proportional Hazards
Everything better on average Calculating sample sizes based on average hazard ratio
Group-sequential stratified weighted log-rank tests in immuno-oncology
Estimands in Practice
Implementing Estimand Framework – Not So Simple!
Roche's estimand journey what we have learned and our future plans
Single World Intervention Graphs for Defining, Identifying, and Communicating Estimands in Clinical Trials
FMS (Swedish Society for Medical Statistics)
Selection bias and multiple inclusion criteria in observational studies
Statistical approaches and considerations when using an external control arm for a rare disease project
Travel vaccines strongly reduce mortality in cancer patients – a real effect or residual confounding
Master Protocols
Bayesian sample size planning for basket trials permitting borrowing of information
Phase II Basket Trials with Pruning and Pooling as Compared to Bayesian Hierarchical Models
Statistical catalysts Influencing an Externally Sponsored platform trial in COVID-19
Platform Trials
Designing an Adaptive Platform Trial in Tuberculosis
Drug combination development to treat infectious diseases Piranga platform trial case study
The EU-PEARL framework to design and conduct platform trials.
The TOGETHER Platform Trial - A multi-center, adaptive, randomized, platform trial to evaluate the effect of repurposed medicines in outpatient
PSI/RSS Prize-Winner's Session
Strategies for improving the assessment of probability of success (PoS) in late stage drug development
Using R for Regulatory Work
Using R for Regulatory Work (combined slides)
Historical Data SIG - framework part 1
Part 1 slides
Launch & Lifecycle SIG - are medical affairs the wild west of statistics
Are medical affairs the wild west of statistics (combined slides)
RWD SIG - Opportunities and Methodological Challenges
Alexander Schacht and Elizabeth Merrall's Slides
Deepak Parashar's slides
Intro slides
The PSI 2022 Conference took place at Gothia Towers, Gothenburg, Sweden from 12th to 15th June.
The conference consisted of a variety of plenary and parallel sessions, as well as breakout discussion sessions, workshops, a poster session and the Annual General Meeting. The conference ran over three full days from Monday to Wednesday, with a choice from two optional half day training course on the Sunday afternoon.
The 2022 Conference was a great success and was the highest attended PSI conference to date. Thank you to everyone involved; speakers, poster presenters, delegates, exhibitors, sponsors, MCI and the PSI scientific committee, for contributing to another successful conference.
David Lawrence, 2022 PSI Conference Chair
Kate Taylor, 2022 PSI Conference Vice-Chair
Paul Terrill, 2021 PSI Conference Vice-Chair
To access the recorded sessions from the PSI 2022 Conference, please visit our Video on Demand homepage.
To source the Conference content, simply select 'PSI 2022 Conference' from the 'Collection' dropdown menu. This will filter all available content to only show on-demand sessions from the 2022 Conference.
Please note: these are only available to view for Members of PSI, and will need to be signed in to watch them.
Some of this year's sessions are unfortunately not available to view on-demand, however we have made the slide decks available. Please see Session Titles listed below, with slide decks available to download beneath.
Please note: these are only accessible for Members of PSI, and will need to be signed in to access them.
Dealing with Non-Proportional Hazards
Everything better on average Calculating sample sizes based on average hazard ratio
Group-sequential stratified weighted log-rank tests in immuno-oncology
Estimands in Practice
Implementing Estimand Framework – Not So Simple!
Roche's estimand journey what we have learned and our future plans
Single World Intervention Graphs for Defining, Identifying, and Communicating Estimands in Clinical Trials
FMS (Swedish Society for Medical Statistics)
Selection bias and multiple inclusion criteria in observational studies
Statistical approaches and considerations when using an external control arm for a rare disease project
Travel vaccines strongly reduce mortality in cancer patients – a real effect or residual confounding
Master Protocols
Bayesian sample size planning for basket trials permitting borrowing of information
Phase II Basket Trials with Pruning and Pooling as Compared to Bayesian Hierarchical Models
Statistical catalysts Influencing an Externally Sponsored platform trial in COVID-19
Platform Trials
Designing an Adaptive Platform Trial in Tuberculosis
Drug combination development to treat infectious diseases Piranga platform trial case study
The EU-PEARL framework to design and conduct platform trials.
The TOGETHER Platform Trial - A multi-center, adaptive, randomized, platform trial to evaluate the effect of repurposed medicines in outpatient
PSI/RSS Prize-Winner's Session
Strategies for improving the assessment of probability of success (PoS) in late stage drug development
Using R for Regulatory Work
Using R for Regulatory Work (combined slides)
Historical Data SIG - framework part 1
Part 1 slides
Launch & Lifecycle SIG - are medical affairs the wild west of statistics
Are medical affairs the wild west of statistics (combined slides)
RWD SIG - Opportunities and Methodological Challenges
Alexander Schacht and Elizabeth Merrall's Slides
Deepak Parashar's slides
Intro slides
The PSI 2022 Conference took place at Gothia Towers, Gothenburg, Sweden from 12th to 15th June.
The conference consisted of a variety of plenary and parallel sessions, as well as breakout discussion sessions, workshops, a poster session and the Annual General Meeting. The conference ran over three full days from Monday to Wednesday, with a choice from two optional half day training course on the Sunday afternoon.
The 2022 Conference was a great success and was the highest attended PSI conference to date. Thank you to everyone involved; speakers, poster presenters, delegates, exhibitors, sponsors, MCI and the PSI scientific committee, for contributing to another successful conference.
David Lawrence, 2022 PSI Conference Chair
Kate Taylor, 2022 PSI Conference Vice-Chair
Paul Terrill, 2021 PSI Conference Vice-Chair
To access the recorded sessions from the PSI 2022 Conference, please visit our Video on Demand homepage.
To source the Conference content, simply select 'PSI 2022 Conference' from the 'Collection' dropdown menu. This will filter all available content to only show on-demand sessions from the 2022 Conference.
Please note: these are only available to view for Members of PSI, and will need to be signed in to watch them.
Some of this year's sessions are unfortunately not available to view on-demand, however we have made the slide decks available. Please see Session Titles listed below, with slide decks available to download beneath.
Please note: these are only accessible for Members of PSI, and will need to be signed in to access them.
Dealing with Non-Proportional Hazards
Everything better on average Calculating sample sizes based on average hazard ratio
Group-sequential stratified weighted log-rank tests in immuno-oncology
Estimands in Practice
Implementing Estimand Framework – Not So Simple!
Roche's estimand journey what we have learned and our future plans
Single World Intervention Graphs for Defining, Identifying, and Communicating Estimands in Clinical Trials
FMS (Swedish Society for Medical Statistics)
Selection bias and multiple inclusion criteria in observational studies
Statistical approaches and considerations when using an external control arm for a rare disease project
Travel vaccines strongly reduce mortality in cancer patients – a real effect or residual confounding
Master Protocols
Bayesian sample size planning for basket trials permitting borrowing of information
Phase II Basket Trials with Pruning and Pooling as Compared to Bayesian Hierarchical Models
Statistical catalysts Influencing an Externally Sponsored platform trial in COVID-19
Platform Trials
Designing an Adaptive Platform Trial in Tuberculosis
Drug combination development to treat infectious diseases Piranga platform trial case study
The EU-PEARL framework to design and conduct platform trials.
The TOGETHER Platform Trial - A multi-center, adaptive, randomized, platform trial to evaluate the effect of repurposed medicines in outpatient
PSI/RSS Prize-Winner's Session
Strategies for improving the assessment of probability of success (PoS) in late stage drug development
Using R for Regulatory Work
Using R for Regulatory Work (combined slides)
Historical Data SIG - framework part 1
Part 1 slides
Launch & Lifecycle SIG - are medical affairs the wild west of statistics
Are medical affairs the wild west of statistics (combined slides)
RWD SIG - Opportunities and Methodological Challenges
Alexander Schacht and Elizabeth Merrall's Slides
Deepak Parashar's slides
Intro slides
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.
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.
Date: Tuesday 9th September 2025 Join us to hear Sofia Weigle and Weng-Kee Wong present their recent work.
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.
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.
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 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.
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).
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: Wednesday 5th November 2025 A careers talk about medical statistics and how it plays a crucial role in developing new medicines
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.
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.
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.
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.
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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