Principal Quantitative Scientist (m/f/d)

Let’s build a healthier future, together! By combining our unique strengths, we are redefining healthcare through sustainable action and innovation. For a behind-the-scenes look, check out this video to see how we at Roche are making personalized health care a reality. The mySugr GmbH was acquired by Roche in 2017 and our Vienna office is one of Roche's global sites. You will be located here, in the heart of Vienna, no matter if you work on a mySugr®, Accu-Chek®, navify® or any other Roche product or solution. You can read more about the history of mySugr & Roche here.Here's what we're looking for:Roche Diagnostics has built a new strategic area – Roche Information Solutions (RIS) - charged with creating a modern portfolio of decision support software products and generating insights that change the way patients are cared for. Our challenge is to bring together complex diagnostic and treatment data from medical devices and IT systems and intelligently process and present this data to clinicians, researchers, and caregivers to improve research outcomes and patient care by offering a suite of Clinical Decision Support (CDS) solutions. We also work with clinical care solutions that are tailored to be used by the patient directly and empower them with the tools to manage their health. As a Principal Quantitative Scientist, you will act as a scientific leader for Real-World Data (RWD), driving evidence generation that fundamentally shapes the development and adoption of our digital health, IVD, and medical device products. This is a high-impact, independent role requiring deep expertise and the ability to influence critical business and regulatory decisions. Your work will involve strategically shaping analyses involving diverse data types (including EHR, claims, omics, and digital health data) in close alignment with data scientists and biostatisticians.Your upcoming mission:RWD Strategy & Execution (End-to-End Leadership): Drive the conceptualization, planning, execution, and reporting of advanced RWD studies using various research and commercial healthcare databases.Develop rigorous RWD study protocols and lead complex analyses to support the evidence needs of the IVD, medical device, and digital health portfolio.Ensure the design, execution, and presentation of RWE adhere to the highest scientific and methodological standards.Strategic Influence & AdoptionAct as a RWD leader, working closely with cross-functional stakeholders such as Product Leads, Medical Affairs, and Clinical Development to ensure RWD projects directly support commercial, market access, and regulatory needs.Champion RWD's use to supplement clinical evidence and actively identify opportunities where RWD can serve as the primary evidence mechanism to achieve regulatory and reimbursement objectives.Collaborate with external partners (KOLs, academic institutions, healthcare authorities) on study design and foster strong relationships to explore new data asse...