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Principal Quantitative Scientist (m/w/d)

Principal Quantitative Scientist (m/w/d)

Principal Quantitative Scientist (m/w/d)

Principal Quantitative Scientist (m/w/d)

Roche

Pharmazeutische Produkte, Arzneimittel

Penzberg

  • Art der Beschäftigung: Vollzeit
  • 93.500 € – 109.500 € (von XING geschätzt)
  • Vor Ort

Principal Quantitative Scientist (m/w/d)

Über diesen Job

JOB DESCRIPTION

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

When we develop diagnostics, pharmaceuticals, or digital products at Roche for the benefit of patients, it is crucial that we can rely on sound data. As a Principal Quantitative Scientist, you play a central role in gaining insights from complex Real World Data (RWD) to support our portfolio of clinical tests and diagnostic devices. Your work contributes directly to better and more efficient patient care and helps us push the boundaries of medical evidence generation.

Your New Team

You will become part of Roche Information Solutions within the Data Science Technologies & Services (DIDT) department. We are a highly specialized team working at the intersection of science and technology. Together, we use state-of-the-art methods in statistics and data processing to generate valuable insights for clinical development, medical departments, product development teams, and regulatory requirements.

Responsibilities | What to Expect

In the role of Principal Quantitative Scientist (m/f/d), you take independent responsibility for the leadership and conception of advanced Real-World Data projects and studies. You are the driver for evidence generation by linking a wide variety of data sources. In doing so, you will take on the following exciting tasks:

  • RWD Study Leadership & Design: You are responsible for the independent planning and execution of RWD studies and create precise study designs as well as Statistical Analysis Plans.

  • Evidence Generation: You coordinate the consolidation of complex data – from patient-level clinical data to omics, imaging, and digital health data.

  • Methodological Development: You develop innovative approaches for using RWD to complement the design of clinical trials or identify opportunities where RWD could be the primary mechanism for generating evidence for regulatory goals.

  • Data Processing & Visualization: You use various programming languages and tools for large-scale processing and visualization of RWD.

  • Strategic Partnerships: You work closely with internal stakeholders (Clinical Development, Medical Affairs) as well as external partners such as key opinion leaders, academic institutions, and CROs.

  • Scientific Presence: You ensure that high-quality study results are published in the form of manuscripts, posters, and abstracts at international congresses to increase the organization's scientific visibility.

Qualifications | What You Bring

  • You have a Master’s degree or a PhD in natural sciences with a focus on statistics (e.g., Epidemiology, Mathematics, or Biostatistics).

  • You have at least 5–7 years (Master’s) or 3–5 years (PhD) of relevant experience in statistical analysis and epidemiology.

  • You possess very good knowledge of statistical programming languages (e.g., R, SAS) and sound knowledge of data management.

  • You bring extensive knowledge of Real World Data study design and are confident working in a regulated/validated environment.

  • You are characterized by excellent communication skills as well as strong stakeholder management abilities.

  • An international, strategic, and goal-oriented mindset, along with a high capacity for learning, defines your working style.

  • You are fluent in both German and English, written and spoken.

So far, so good? It gets even better.

We offer you a variety of top benefits at our locations. Only together with you can we improve the lives of patients. Your contribution makes Roche unique. That’s why we offer extraordinary benefits that support you in shaping your life, finances, and health exactly the way you want. Find out more here: https://go.roche.com/Kandidaten-Benefits-DE

Duration: This position is permanent (unbefristet).

Do you want to become part of a dynamic team and significantly shape the success in Penzberg? Then apply now!

Your Application

Please provide us with the following documents:

  • Current CV or an updated Workday profile

  • Relevant certificates and evidence of your qualifications

Further documents are not mandatory at this stage. Please note that no further documents can be added after the application has been submitted.

Apply now – we look forward to meeting you!

Do you need further support?

Please have a look at our FAQs, you will find them via https://careers.roche.com/global/en/faq .

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

Gehalts-Prognose

Unternehmens-Details

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Roche

Pharmazeutische Produkte, Arzneimittel

10.001 oder mehr Mitarbeitende

Basel, Schweiz

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