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Marina Zanatta
Meet Our DIGICORE Community
Marina Zanatta, PhD
Biostatistician
INOC - Istituto Nazionale Oncologico Candiolo
Based in Turin, INOC is an OECI Comprehensive Cancer Centre and oncological IRCCS, and serves as a reference centre for nine tumour types. Operating since 1996, the institute’s mission has been to integrate clinical assistance and translational research to advance cancer diagnosis and treatment.
“I am driven by the idea that rigorous data analysis can turn real-world complexity into meaningful evidence, helping multidisciplinary teams translate clinical and research ideas into robust study designs.”
What drew you to RWE, precision oncology or digital health?
My interest in RWE comes mainly from my work as a biostatistician. I was trained in biostatistics, with a strong focus on study design and data analysis. After my master I started working with administrative data and I have realized that there is so much information in data that are not collected for research purpose. This made me interested in RWE as a way to complement evidence from clinical trials and answer questions that are difficult to address in controlled settings.
What is your professional background & training?
I have a background in biostatistics, with academic training focused on statistical methods, study design and data analysis. My professional experience has been in data analysis and clinical research, particularly in oncology, where I work closely with clinicians and researchers on the design and analysis of clinical studies, as well as on scientific writing. My training has given me a strong methodological background, while my work in a clinical setting has allowed me to understand the practical challenges of working with real clinical data.
What does your current role involve?
I currently work as a biostatistician at INOC, a CCC and oncological IRCCS. My role covers different stages of clinical research, from study design and definition of statistical methods to data cleaning, analysis and interpretation of results. I work closely with clinicians and researchers on clinical trials and observational studies, and I also contribute to scientific publications. Working directly with clinical data has made me increasingly interested in how routinely collected data can be used to generate reliable evidence.
What are you working towards, and what comes next?
I would like to deepen my expertise in RWE and develop a stronger understanding of how to design and analyse studies based on real-world data.
What advice do you have for someone who is interested in moving into this field?
I would suggest starting from a solid understanding of study design and statistical methods, but also spending time learning how clinical data are actually generated and used in practice. RWE requires more than knowing statistical techniques: understanding the clinical context and the strengths and limitations of the data is essential. I would also encourage people to work closely with clinicians and researchers from different backgrounds, because many of the most interesting questions emerge from these multidisciplinary collaborations.
What's one thing people would never guess about your work?
One thing people may never guess about my work is how creative statistics and study design can be. There are certainly a lot of numbers involved, but there is also quite a lot of imagination. Designing a study often means finding creative ways to turn a clinical question into something that can actually be studied, while working within practical constraints. I find this combination of analytical thinking and creativity one of the most interesting parts of being a biostatistician.
Research interests
Biostatistics
Epidemiology
Study design
Methodology
Real World Evidence
Regression models
Casual inference
Survival
RCTs