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From Raw Data to Regulatory Results: Clinical Trial Programming in R using the pharmaverse workshop

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Join our workshop on From Raw Data to Regulatory Results: Clinical Trial Programming in R using the pharmaverse,  which is a part of our workshops for Ukraine series! 


Here’s some more info: 


Title: From Raw Data to Regulatory Results: Clinical Trial Programming in R using the pharmaverse

Date: Thursday, September 17th, 18:00 – 20:00 CEST (Rome, Berlin, Paris timezone) 

Speaker: Edoardo Mancini, Edoardo is a Senior Data Scientist working at Roche in the UK. His work involves leading statistical programming activities in early and late-stage clinical trials across multiple therapeutic areas, including Ophthalmology and Hematology. Edoardo is also a passionate advocate for R and Open Source, pursuing these interests in his current role as maintainer for the open-source {admiral} R package, which is part of the wider pharmaverse and helps create ADaM datasets. 

Description: Have you ever wondered how raw patient data from a clinical trial transforms into the actual evidence used to approve new medicines? This two-hour, hands-on workshop aims to answer this question by giving you a glimpse into the clinical trial data pipeline. We’ll start with a crash course on industry data standards, tracing the journey from raw data to SDTM (Study Data Tabulation Model), into analysis-ready ADaM datasets, and finally into Tables, Listings, and Graphs (TLGs). From there, you will step into the shoes of a clinical statistical programmer: firstly, you will be guided through creating your own simple ADaM dataset(s) using the {admiral} package and test data. Then, you will bring your analyses to life using {ggplot2} and a tabulation package of your choice to build the kinds of polished visualizations and summary tables that drive real-world medical breakthroughs. No prior clinical trial experience is required, just bring your foundational R skills and your curiosity!

Minimal registration fee: 20 euro (or 20 USD or 800 UAH)


Please note that the registration confirmation is sent 1 day before the workshop to all registered participants rather than immediately after registration


How can I register?





If you are not personally interested in attending, you can also contribute by sponsoring a participation of a student, who will then be able to participate for free. If you choose to sponsor a student, all proceeds will also go directly to organisations working in Ukraine. You can either sponsor a particular student or you can leave it up to us so that we can allocate the sponsored place to students who have signed up for the waiting list.


How can I sponsor a student?





If you are a university student and cannot afford the registration fee, you can also sign up for the waiting list here. (Note that you are not guaranteed to participate by signing up for the waiting list).



You can also find more information about this workshop series,  a schedule of our future workshops as well as a list of our past workshops which you can get the recordings & materials here.


Looking forward to seeing you during the workshop!










 


















From Raw Data to Regulatory Results: Clinical Trial Programming in R using the pharmaverse workshop was first posted on August 12, 2026 at 3:03 pm.
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