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
PSI Introduction to Industry Training (ITIT) Course - 2026/2027
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.
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 webinar brings together three bitesize complementary sessions to help PSI contributors create conference presentations and posters that communicate clearly and inclusively. Participants will explore how to refine their message, prepare materials effectively, and adopt practical habits that support confident, accessible delivery. A focused, supportive session designed to elevate every contribution.
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, “Graphics Basics,” will introduce the fundamentals of producing graphics using the ggplot2 package.
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.
Join our Health Technology Assessment (HTA) European Special Interest Group (ESIG) for a webinar on the strategic role of statisticians in the Joint Clinical Assessment (JCA). The introduction of the JCA marks a new era for evidence generation and market access in Europe. As HTA requirements become more harmonized and methodologically demanding, the role of statisticians has evolved far beyond data analysis. Today, statistical expertise is central to shaping clinical development strategies, designing robust comparative evidence, and ensuring that submissions withstand the scrutiny of EU-level assessors. In this webinar, we explore how statisticians contribute strategically to successful JCA outcomes.
Statisticians in the Age of AI: On Route to Strategic Partnership
A 90-minute webinar featuring two case studies from Bayer and Roche demonstrating how statisticians successfully integrated into AI programs, followed by interactive discussion on strategies for elevating statistical expertise in the AI era.
Enhancing Clinical Study Reporting with the Estimand Framework
Join us for an insightful webinar where we explore practical strategies for applying the estimand framework in clinical study reporting. Drawing on real-world experiences and case studies, we will share recommendations to help you:
• Understand the role of estimands in improving transparency and interpretation of trial results.
• Navigate common challenges in implementing the framework during reporting.
• Apply best practices to enhance regulatory submissions, webposting in public registries (clinicaltrials.gov/CTIS), and scientific publications.
Whether you are involved in clinical trial design, data analysis, or regulatory submissions, this session will provide actionable guidance to realize the full potential of the estimand framework.
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 networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
GSK - Statistics Director - Vaccines and Infectious Disease
We are seeking an experienced and visionary Statistics Director to join our Team and lead strategic statistical innovation across GSK’s Vaccines and Infectious Disease portfolio.
As a Senior Biostatistician I at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
As a Statistical Scientist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
We have an exciting opportunity for an Associate Director, Biostatistics to join a passionate team within Advanced Quantitative Sciences – Full Development.
: We have an exciting opportunity for an Associate Director (AD), Statistical Programming, to join a passionate team within Advanced Quantitative Sciences- Development.
Novartis - Senior Principal Statistical Programmer
We have an exciting opportunity for a Senior Principal Statistical Programmer, to join a passionate team within Advanced Quantitative Sciences – Development.
Pierre Fabre - Clinical Development Safety Statistics Expert M/F
We are seeking a highly skilled and proactive Clinical Development Safety Statistics Expert to join our Biometry Department and the Biometry Leadership Team based in Toulouse (31, Oncopole) or Boulogne (92).
Pierre Fabre - Lead Statistician – Real World Evidence -CDI- M/F
Pierre Fabre Laboratories are hiring a highly skilled and experienced Lead Statistician – Real World Evidence (RWE) to join the Biometry Department, part of the Data Science & Biometry Department, based in Toulouse (Oncopôle) or Boulogne.
Pierre Fabre - Lead Statistician- Clinical Trials M/F
We are seeking a highly skilled and experienced Lead Statistician in Clinical Trials to join our Biometry Department based in Toulouse (31, Oncopole) or Boulogne (92).
We are looking for Senior Statistical Programmers in the UK to join Veramed, where you'll deliver high-impact programming solutions in an FSP-style capacity, while advancing your career in a supportive, growth-driven environment.