Location:
Online via Zoom Speakers:
The training course will be led by Sue McKendrick, Statistical Science Director in PPD™.
Additional presenters, tutors and panellists will participate across different sessions over the 4 days, including: Who is this event intended for? Clinical Statisticians who wish to facilitate the effective implementation of the estimand framework in clinical trial protocols, and understand the challenges in design, data collection, estimation and reporting.
Due to the interactive nature of this online workshop, there are a limited number of places so please apply quickly to avoid disappointment. Whilst the estimand framework can apply to any phase of clinical trial, we will focus mostly on Phase 2 and 3.
What is the benefit of attending? Since the implementation of ICH E9(R1), estimands have become a critical foundation to the development of clinical trials. Delegates will gain experience of applying the estimand framework to real case studies. The training will give an opportunity to discuss estimands with experts from the estimand implementation working group (EIWG) and gain the skills to discuss and apply the estimand framework to their own studies.
Cost
Early Bird PSI Members = £320+VAT PSI Members = £360+VAT
Early Bird Non-Members = £430+VAT Non-Members = £470+VAT
*Please note: Non-Member rates include PSI membership until 31 Dec. 2025.
Registration
To book your place, please click here. Early Bird rates end on Monday 10th February.
Overview: Experts from the Estimand Implementation Working Group (EIWG) will provide an in-depth review of the estimand framework as laid out by ICH E9(R1) addendum. Case studies will be discussed illustrating the implementation of this framework in a variety of settings and therapeutic areas, and equivalence, non-inferiority and superiority goals. Insights into the best practice for handling intercurrent events in data will be provided by the PHUSE Implementation of Estimands using Data Standards Project Team.
In addition, we will engage delegates through considering how estimands might apply to their own clinical settings, interactive quizzes and break out rooms for team discussions of a case study. To get the most from this training, delegates should be prepared to switch on cameras for discussions and complete some tasks between sessions. Team discussions will be supported by EIWG tutors.
Location:
Online via Zoom Speakers:
The training course will be led by Sue McKendrick, Statistical Science Director in PPD™.
Additional presenters, tutors and panellists will participate across different sessions over the 4 days, including: Who is this event intended for? Clinical Statisticians who wish to facilitate the effective implementation of the estimand framework in clinical trial protocols, and understand the challenges in design, data collection, estimation and reporting.
Due to the interactive nature of this online workshop, there are a limited number of places so please apply quickly to avoid disappointment. Whilst the estimand framework can apply to any phase of clinical trial, we will focus mostly on Phase 2 and 3.
What is the benefit of attending? Since the implementation of ICH E9(R1), estimands have become a critical foundation to the development of clinical trials. Delegates will gain experience of applying the estimand framework to real case studies. The training will give an opportunity to discuss estimands with experts from the estimand implementation working group (EIWG) and gain the skills to discuss and apply the estimand framework to their own studies.
Cost
Early Bird PSI Members = £320+VAT PSI Members = £360+VAT
Early Bird Non-Members = £430+VAT Non-Members = £470+VAT
*Please note: Non-Member rates include PSI membership until 31 Dec. 2025.
Registration
To book your place, please click here. Early Bird rates end on Monday 10th February.
Overview: Experts from the Estimand Implementation Working Group (EIWG) will provide an in-depth review of the estimand framework as laid out by ICH E9(R1) addendum. Case studies will be discussed illustrating the implementation of this framework in a variety of settings and therapeutic areas, and equivalence, non-inferiority and superiority goals. Insights into the best practice for handling intercurrent events in data will be provided by the PHUSE Implementation of Estimands using Data Standards Project Team.
In addition, we will engage delegates through considering how estimands might apply to their own clinical settings, interactive quizzes and break out rooms for team discussions of a case study. To get the most from this training, delegates should be prepared to switch on cameras for discussions and complete some tasks between sessions. Team discussions will be supported by EIWG tutors.
Location:
Online via Zoom Speakers:
The training course will be led by Sue McKendrick, Statistical Science Director in PPD™.
Additional presenters, tutors and panellists will participate across different sessions over the 4 days, including: Who is this event intended for? Clinical Statisticians who wish to facilitate the effective implementation of the estimand framework in clinical trial protocols, and understand the challenges in design, data collection, estimation and reporting.
Due to the interactive nature of this online workshop, there are a limited number of places so please apply quickly to avoid disappointment. Whilst the estimand framework can apply to any phase of clinical trial, we will focus mostly on Phase 2 and 3.
What is the benefit of attending? Since the implementation of ICH E9(R1), estimands have become a critical foundation to the development of clinical trials. Delegates will gain experience of applying the estimand framework to real case studies. The training will give an opportunity to discuss estimands with experts from the estimand implementation working group (EIWG) and gain the skills to discuss and apply the estimand framework to their own studies.
Cost
Early Bird PSI Members = £320+VAT PSI Members = £360+VAT
Early Bird Non-Members = £430+VAT Non-Members = £470+VAT
*Please note: Non-Member rates include PSI membership until 31 Dec. 2025.
Registration
To book your place, please click here. Early Bird rates end on Monday 10th February.
Overview: Experts from the Estimand Implementation Working Group (EIWG) will provide an in-depth review of the estimand framework as laid out by ICH E9(R1) addendum. Case studies will be discussed illustrating the implementation of this framework in a variety of settings and therapeutic areas, and equivalence, non-inferiority and superiority goals. Insights into the best practice for handling intercurrent events in data will be provided by the PHUSE Implementation of Estimands using Data Standards Project Team.
In addition, we will engage delegates through considering how estimands might apply to their own clinical settings, interactive quizzes and break out rooms for team discussions of a case study. To get the most from this training, delegates should be prepared to switch on cameras for discussions and complete some tasks between sessions. Team discussions will be supported by EIWG tutors.
Location:
Online via Zoom Speakers:
The training course will be led by Sue McKendrick, Statistical Science Director in PPD™.
Additional presenters, tutors and panellists will participate across different sessions over the 4 days, including: Who is this event intended for? Clinical Statisticians who wish to facilitate the effective implementation of the estimand framework in clinical trial protocols, and understand the challenges in design, data collection, estimation and reporting.
Due to the interactive nature of this online workshop, there are a limited number of places so please apply quickly to avoid disappointment. Whilst the estimand framework can apply to any phase of clinical trial, we will focus mostly on Phase 2 and 3.
What is the benefit of attending? Since the implementation of ICH E9(R1), estimands have become a critical foundation to the development of clinical trials. Delegates will gain experience of applying the estimand framework to real case studies. The training will give an opportunity to discuss estimands with experts from the estimand implementation working group (EIWG) and gain the skills to discuss and apply the estimand framework to their own studies.
Cost
Early Bird PSI Members = £320+VAT PSI Members = £360+VAT
Early Bird Non-Members = £430+VAT Non-Members = £470+VAT
*Please note: Non-Member rates include PSI membership until 31 Dec. 2025.
Registration
To book your place, please click here. Early Bird rates end on Monday 10th February.
Overview: Experts from the Estimand Implementation Working Group (EIWG) will provide an in-depth review of the estimand framework as laid out by ICH E9(R1) addendum. Case studies will be discussed illustrating the implementation of this framework in a variety of settings and therapeutic areas, and equivalence, non-inferiority and superiority goals. Insights into the best practice for handling intercurrent events in data will be provided by the PHUSE Implementation of Estimands using Data Standards Project Team.
In addition, we will engage delegates through considering how estimands might apply to their own clinical settings, interactive quizzes and break out rooms for team discussions of a case study. To get the most from this training, delegates should be prepared to switch on cameras for discussions and complete some tasks between sessions. Team discussions will be supported by EIWG tutors.
Location:
Online via Zoom Speakers:
The training course will be led by Sue McKendrick, Statistical Science Director in PPD™.
Additional presenters, tutors and panellists will participate across different sessions over the 4 days, including: Who is this event intended for? Clinical Statisticians who wish to facilitate the effective implementation of the estimand framework in clinical trial protocols, and understand the challenges in design, data collection, estimation and reporting.
Due to the interactive nature of this online workshop, there are a limited number of places so please apply quickly to avoid disappointment. Whilst the estimand framework can apply to any phase of clinical trial, we will focus mostly on Phase 2 and 3.
What is the benefit of attending? Since the implementation of ICH E9(R1), estimands have become a critical foundation to the development of clinical trials. Delegates will gain experience of applying the estimand framework to real case studies. The training will give an opportunity to discuss estimands with experts from the estimand implementation working group (EIWG) and gain the skills to discuss and apply the estimand framework to their own studies.
Cost
Early Bird PSI Members = £320+VAT PSI Members = £360+VAT
Early Bird Non-Members = £430+VAT Non-Members = £470+VAT
*Please note: Non-Member rates include PSI membership until 31 Dec. 2025.
Registration
To book your place, please click here. Early Bird rates end on Monday 10th February.
Overview: Experts from the Estimand Implementation Working Group (EIWG) will provide an in-depth review of the estimand framework as laid out by ICH E9(R1) addendum. Case studies will be discussed illustrating the implementation of this framework in a variety of settings and therapeutic areas, and equivalence, non-inferiority and superiority goals. Insights into the best practice for handling intercurrent events in data will be provided by the PHUSE Implementation of Estimands using Data Standards Project Team.
In addition, we will engage delegates through considering how estimands might apply to their own clinical settings, interactive quizzes and break out rooms for team discussions of a case study. To get the most from this training, delegates should be prepared to switch on cameras for discussions and complete some tasks between sessions. Team discussions will be supported by EIWG tutors.
Location:
Online via Zoom Speakers:
The training course will be led by Sue McKendrick, Statistical Science Director in PPD™.
Additional presenters, tutors and panellists will participate across different sessions over the 4 days, including: Who is this event intended for? Clinical Statisticians who wish to facilitate the effective implementation of the estimand framework in clinical trial protocols, and understand the challenges in design, data collection, estimation and reporting.
Due to the interactive nature of this online workshop, there are a limited number of places so please apply quickly to avoid disappointment. Whilst the estimand framework can apply to any phase of clinical trial, we will focus mostly on Phase 2 and 3.
What is the benefit of attending? Since the implementation of ICH E9(R1), estimands have become a critical foundation to the development of clinical trials. Delegates will gain experience of applying the estimand framework to real case studies. The training will give an opportunity to discuss estimands with experts from the estimand implementation working group (EIWG) and gain the skills to discuss and apply the estimand framework to their own studies.
Cost
Early Bird PSI Members = £320+VAT PSI Members = £360+VAT
Early Bird Non-Members = £430+VAT Non-Members = £470+VAT
*Please note: Non-Member rates include PSI membership until 31 Dec. 2025.
Registration
To book your place, please click here. Early Bird rates end on Monday 10th February.
Overview: Experts from the Estimand Implementation Working Group (EIWG) will provide an in-depth review of the estimand framework as laid out by ICH E9(R1) addendum. Case studies will be discussed illustrating the implementation of this framework in a variety of settings and therapeutic areas, and equivalence, non-inferiority and superiority goals. Insights into the best practice for handling intercurrent events in data will be provided by the PHUSE Implementation of Estimands using Data Standards Project Team.
In addition, we will engage delegates through considering how estimands might apply to their own clinical settings, interactive quizzes and break out rooms for team discussions of a case study. To get the most from this training, delegates should be prepared to switch on cameras for discussions and complete some tasks between sessions. Team discussions will be supported by EIWG tutors.
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.
Topic: R Package Basics.
Our monthly webinar series allows attendees to gain practical knowledge and skills in open-source coding and tools, with a focus on applications in the pharmaceutical industry. This month’s session, “R Package Basics,” will introduce the fundamentals of working with R packages—covering how to install, load, and manage them effectively to support data analysis and reproducible research. The session will provide a solid starting point, clarify common misconceptions, and offer valuable resources for continued learning.
Date: Ongoing 6 month cycle beginning late April/early May 2026
Are you a member of PSI looking to further your career or help develop others - why not sign up to the PSI Mentoring scheme? You can expand your network, improve your leadership skills and learn from more senior colleagues in the industry.
PSI Book Club Lunch and Learn: Communicating with Clarity and Confidence
If you have read Ros Atkins’ book The Art of Explanation or want to listen to the BBC’s ‘Communicator in Chief’, you are invited to join the PSI Book Club Lunch and Learn, to discuss the content and application with the author, Ros Atkins. Having written the book within the context of the news industry, Ros is keen to hear how we have applied the ideas as statisticians within drug development and clinical trials. There will be dedicated time during the webinar to ASK THE AUTHOR any questions – don’t miss out on this exclusive PSI Book Club event!
Haven’t read the book yet? Pick up a copy today and join us.
Explanation - identifying and communicating what we want to say - is described as an art, in the title of his book. However, the creativity comes from Ros’ discernment in identifying and describing a clear step-by-step process to follow and practice. Readers can learn Ros’ rules, developed and polished throughout his career as a journalist, to help communicate complex written or spoken information clearly.
PSI Training Course: Effective Leadership – the keys to growing your leadership capabilities
This course will consist of three online half-day workshops. The first will be aimed at building trust, the backbone of leadership and a key to becoming effective. This is key to building a solid foundation.
The second will be on improving communication as a technical leader. This workshop will focus on communication strategies for different stakeholders and will involve tips on effective communication and how to develop the skills of active listening, coaching and what improv can teach us about good communication.
The final workshop will bring these two components together to help leaders become more influential. This will also focus on how to use Steven Covey’s 7-Habits, in particular Habits 4, 5 and 6, which are called the habits of communication.
The workshops will be interactive, allowing you to practice the concepts discussed. There will be plenty of time for questions and discussion. There will also be reflective time where you can think about what you are learning and how you might experiment with it.