Dates & Times:
Module 1 - Monday 10th March: 09:30-15:00 BST
Module 2 - Thursday 20th March: 09:30-15:00 BST
Module 3 - Friday 21st March: 09:30-15:00 BST
Module 4 - Friday 28th March: 09:00-15:00 BST
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.
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.
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.
Dates & Times:
Module 1 - Monday 10th March: 09:30-15:00 BST
Module 2 - Thursday 20th March: 09:30-15:00 BST
Module 3 - Friday 21st March: 09:30-15:00 BST
Module 4 - Friday 28th March: 09:00-15:00 BST
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.
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.
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.
Dates & Times:
Module 1 - Monday 10th March: 09:30-15:00 BST
Module 2 - Thursday 20th March: 09:30-15:00 BST
Module 3 - Friday 21st March: 09:30-15:00 BST
Module 4 - Friday 28th March: 09:00-15:00 BST
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.
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.
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.
Dates & Times:
Module 1 - Monday 10th March: 09:30-15:00 BST
Module 2 - Thursday 20th March: 09:30-15:00 BST
Module 3 - Friday 21st March: 09:30-15:00 BST
Module 4 - Friday 28th March: 09:00-15:00 BST
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.
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.
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.
Dates & Times:
Module 1 - Monday 10th March: 09:30-15:00 BST
Module 2 - Thursday 20th March: 09:30-15:00 BST
Module 3 - Friday 21st March: 09:30-15:00 BST
Module 4 - Friday 28th March: 09:00-15:00 BST
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.
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.
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.
Dates & Times:
Module 1 - Monday 10th March: 09:30-15:00 BST
Module 2 - Thursday 20th March: 09:30-15:00 BST
Module 3 - Friday 21st March: 09:30-15:00 BST
Module 4 - Friday 28th March: 09:00-15:00 BST
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.
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.
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.
An introductory course giving an overview of the pharmaceutical industry and the drug development process as a whole, aimed at those with 1-3 years' experience. It comprises of six 2-day sessions covering a range of topics including Research and Development, Toxicology, Data Management and the Role of a CRO, Clinical Trials, Reimbursement, and Marketing.
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.
The book club’s usual focus is to read and discuss professional development books. In this short format event you can more easily develop you career without the commitment of reading the whole book - simply listen to the 1-hour long podcast before joining the interactive session on 21 May.
This webinar is organised by the RWD SIG and the Historical Data SIG. We will review recent methods, applications, and tools of integrating subject-level-data from clinical trial with external data using Bayesian methods and/or causal inference methods.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
This will be a 45 minute webinar which will explain the topic presented in the published paper, ‘Applying the Estimand Framework to Clinical Pharmacology Trials with a Case Study in Bioequivalance’. There will be 15 minutes for a panel Q&A with some of the authors following the presentation.
This 1-hour webinar will be an opportunity to hear about the methodology and first results of the iRISE consortium. iRISE is working towards a better understanding of reproducibility and the interventions that work to improve it. At the end of the presentation there will also be the opportunity to ask questions.
This one-day event focuses on the comprehensive management of transitioning to R/Open-Source, addressing the challenges and providing actionable insights. Attendees will participate in sessions covering essential topics such as training best practices, creating strategic plans, making the case to senior management, and managing both statistical and programming aspects of the transition.
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.
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.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
The Institute of Cancer Research are seeking to appoint a Research Group Leader to join The CRUK Clinical Trials and Statistics Unit at the ICR.
This is an exciting, new opportunity for an experienced Statistician looking to take the next step in their career. Offered as a remote or hybrid position aligned with our site in Harrogate, North Yorkshire.
The BioMarin internship programme will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin, whilst gaining an insight into the pharmaceutical/biotech industry.
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