Estimands: From Protocol to Analysis
Unlock the power of estimands in clinical research! Join our second upcoming webinar to learn how the estimand framework is revolutionising the way we define and analyse research questions.
We’ll explain the concept of estimands, explore strategies for handling intercurrent events, and showcase real-world examples of how interdisciplinary collaboration is key to achieving valid inferences.
📅 Date: Tuesday 15th October 2024
🕒 Time: 2:30-4:30pm Paris time
🎙️Elodie Blondiaux and Stéphane Verdun
👥 Hosted by: Venn Life Sciences
🔑 Key Learnings:
• What exactly is an estimand?
• Who is responsible for defining estimands?
• Why is precise definition so critical?
• Effective strategies for managing intercurrent events
About the Speakers:
Elodie Blondiaux
A biostatistician by training, Elodie has 15 years of experience in Clinical Development of pharmaceutical products and diagnostics devices. She started her career as a statistician with Sanofi in late phase trials before moving to the CRO business where she was involved in a wide range of clinical trials from Phase I to Phase IV and non-interventional studies. She has worked in several therapeutic areas, including cardiology, haematology, infectious diseases, gene therapy, and rare diseases. Her experience covers all aspects of biostatistical activities in pharmaceutical industry, including methodology and design of clinical trials, as well as statistical support of clinical trial conduct itself as statistical analysis plan writing and data analysis.
Stéphane Verdun
After a PhD in Applied Statistics, Stéphane headed the biostatistics unit at a small #biotech, working with laboratory and genomics data to develop models to diagnose cancer and predict cancer severity. He then spent 7 years in the Delegation for Clinical Research and Innovation of Lille Catholic Hospitals, supporting all statistical activities from the definition of research questions and project methodology all the way to reporting and co-authoring scientific publications. These include estimating sample size, analysis trials results, developing protocols, writing and reviewing of SAP, just to name a few. In this role, he focused on late phase, retrospective or RWE studies. His activities now in Venn Life Sciences cover a large range of biostatistical activities, from handling data in CDISC format, programming simple or complex statistical analyses, as well as bringing input on statistical methodology, clinical trials design and estimand definitions.
🎟️ Registration: FREE of charge
Gain practical insights to ensure your study protocols align seamlessly with research objectives, setting the stage for successful outcomes.
🚀 Don’t miss this opportunity to sharpen your clinical research skills!
🔔 Stay Tuned: Follow this event for updates and announcements about upcoming free webinars.
You can view this webinar from your computer, tablet or mobile phone.
We’ll explain the concept of estimands, explore strategies for handling intercurrent events, and showcase real-world examples of how interdisciplinary collaboration is key to achieving valid inferences.
📅 Date: Tuesday 15th October 2024
🕒 Time: 2:30-4:30pm Paris time
🎙️Elodie Blondiaux and Stéphane Verdun
👥 Hosted by: Venn Life Sciences
🔑 Key Learnings:
• What exactly is an estimand?
• Who is responsible for defining estimands?
• Why is precise definition so critical?
• Effective strategies for managing intercurrent events
About the Speakers:
Elodie Blondiaux
A biostatistician by training, Elodie has 15 years of experience in Clinical Development of pharmaceutical products and diagnostics devices. She started her career as a statistician with Sanofi in late phase trials before moving to the CRO business where she was involved in a wide range of clinical trials from Phase I to Phase IV and non-interventional studies. She has worked in several therapeutic areas, including cardiology, haematology, infectious diseases, gene therapy, and rare diseases. Her experience covers all aspects of biostatistical activities in pharmaceutical industry, including methodology and design of clinical trials, as well as statistical support of clinical trial conduct itself as statistical analysis plan writing and data analysis.
Stéphane Verdun
After a PhD in Applied Statistics, Stéphane headed the biostatistics unit at a small #biotech, working with laboratory and genomics data to develop models to diagnose cancer and predict cancer severity. He then spent 7 years in the Delegation for Clinical Research and Innovation of Lille Catholic Hospitals, supporting all statistical activities from the definition of research questions and project methodology all the way to reporting and co-authoring scientific publications. These include estimating sample size, analysis trials results, developing protocols, writing and reviewing of SAP, just to name a few. In this role, he focused on late phase, retrospective or RWE studies. His activities now in Venn Life Sciences cover a large range of biostatistical activities, from handling data in CDISC format, programming simple or complex statistical analyses, as well as bringing input on statistical methodology, clinical trials design and estimand definitions.
🎟️ Registration: FREE of charge
Gain practical insights to ensure your study protocols align seamlessly with research objectives, setting the stage for successful outcomes.
🚀 Don’t miss this opportunity to sharpen your clinical research skills!
🔔 Stay Tuned: Follow this event for updates and announcements about upcoming free webinars.
You can view this webinar from your computer, tablet or mobile phone.
