Hurricanes, Elections and Clinical Trials:Some Novel Approaches to Visualising Uncertainty
This animation is known as a Hypothetical Outcome Plot (HOP) which can be effective in communicating inferential uncertainty to an audience without statistical training. Such novel data visualisation methods are common in fields such as election forecasting and hurricane prediction, but quite underutilised in clinical trial reporting. Webinar Weather, Elections and Clinical Trials: Some novel […]
Statistician Types: Otis Rimmer, from Programmer to Technical Statistician
Have you ever felt pigeonholed in your career? Wanted to make a change but weren’t sure if you would suit a new role? Progressing or shifting one’s career in the bio-pharmaceutical industry can be a challenging and, at times, uncertain path to travel. Roles and sectors can feel rigid. Some find that once they’ve gone […]
Addressing new EU HTA legislation in 2024: A case study on Estimands and PICOs
Oncology trials starts have reached unprecedented levels, with a 56% increase from 2016 to 2021. From the 15,267 assets that were in development in 2021, 34% were oncology. However, an alarming concern arises when we question the involvement of market access experts and Statisticians in the complete development lifecycle. It is common practice for these […]
Data Visualization Webinars
With tightening margins and deadlines facing today’s clinical trial journeys, the need to communicate and share data through powerful visualizations is paramount. Watch our latest Data Visualization Webinar to discover the future of data visualization in the bio-pharma space and how to tackle common industry challenges. April, 2023 Data Visualizations: tips to connect with your […]
The rise of data visualisation: from hot topic to true innovation
Data visualisation has become a hot topic within the biostatistics space, especially over the past few years. The PSI conference in Gothenburg earlier this year showed us all just how hot it is, as there was a considerable improvement and uptick in the use of data visualisations across all presentations and posters at the conference. […]
Forging a better commercialisation pathway through real world evidence generation
By Rachel Tham, Senior Statistician Real world evidence generation is playing an increasingly important role in enabling sponsors to gain better insights across a range of scenarios to improve the patient experience. At Veramed our Launch and Commercialisation business unit draws on our team’s extensive experience both internally and within sponsor organisations, supporting evidence generation […]
Preparing your remedy for market: surprising insight from the sales team
The role of the sales team within the Launch and Commercialisation space can often be misleading. While the function of sales is no different to many other industries, the approach to market, and working with physicians and payers requires a real understanding of customer needs and product insight. Many years ago, I spent a day […]
Plotting a career path to senior programmer
Our career profile series highlights the career journeys of members of our team and illustrates the variety of progression routes and opportunities available to statisticians and programmers at Veramed. In this profile, we sit down with James Diserens, a Senior Programmer at Veramed, and discuss his career path to date, his motivations, and his aspirations […]
First Time Lead Programmers: Randomised Clinical Trials vs Real World Evidence Studies
Learn more about Randomised Clinical Trials and Real World Evidence Studies and get tips on becoming a Lead Programmer. Presented by Kirsty Parker-Hodds and Anisa Jeetoo.If you liked this webinar, you can download a copy of the slides by entering your details below.JTNDaWZyYW1lJTIwc3JjJTNEJTIyaHR0cHMlM0ElMkYlMkZnby52ZXJhbWVkLmNvLnVrJTJGbCUyRjg2MDU1MyUyRjIwMjAtMTAtMDclMkZ5Zmh4JTIyJTIwd2lkdGglM0QlMjIxMDAlMjUlMjIlMjBoZWlnaHQlM0QlMjI1MDAlMjIlMjB0eXBlJTNEJTIydGV4dCUyRmh0bWwlMjIlMjBmcmFtZWJvcmRlciUzRCUyMjAlMjIlMjBhbGxvd1RyYW5zcGFyZW5jeSUzRCUyMnRydWUlMjIlMjBzdHlsZSUzRCUyMmJvcmRlciUzQSUyMDAlMjIlM0UlM0MlMkZpZnJhbWUlM0U=
How a targeted approach can ease the CDISC compliance burden
“Whenever you want to achieve something, keep your eyes open, concentrate and make sure you know exactly what it is you want. No one can hit their target with their eyes closed.” Paulo Coelho Since the FDA mandated that sponsors with studies starting after December 17, 2016 should submit data in FDA-supported formats, familiarity with the […]