About this role
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.
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The Position
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche
The Opportunity
- Partner across clinical teams: Collaborate directly with clinical investigators and research partners to design robust clinical studies, select sound statistical methodologies, and ensure appropriate sample sizes that substantiate clinical utility.
- Author critical study documentation: Write comprehensive statistical analysis plans (SAPs) and detailed statistical reports for health authority review and scientific evaluation.
- Deliver end-to-end analytical rigor : Perform high-quality data analyses, coordinate sample randomization and blinding procedures, and oversee peer quality reviews (QC) to uphold rigorous data integrity.
- Drive methodological innovation: Identify, develop, and apply novel statistical solutions and study design improvements to address complex technical challenges in diagnostic development.
- Mentor and cultivate expertise: Take ownership of major diagnostic project deliverables while coaching and empowering team members to advance collective statistical capabilities.
- Share knowledge broadly: Represent the team’s scientific contributions through technical publications, conference presentations, and cross-functional workshops.
Who You Are
- You bring a Master’s degree in Statistics, Biostatistics, or a closely related quantitative field with 9+ years of relevant experience (or a PhD with 6+ years).
- You possess hands-on proficiency in statistical programming with SAS or R, alongside a track record of statistical analysis and reporting for diagnostic validation or clinical studies.
- You demonstrate practical understanding of regulatory considerations for in vitro diagnostic (IVD) devices, including sensitivity, specificity, agreement rates, and reproducibility evaluations.
- You thrive in collaborative, multi-disciplinary team environments where cross-functional alignment and coordinated quality control are central to success.
- You communicate statistical concepts clearly and effectively to diverse scientific audiences, supported by technical presentations, white papers, or publications
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The expected salary range for this position based on the primary location of Indianapolis, IN is 102,500-190,300 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance.
This position also qualifies for the benefits detailed at the link provided below.
Benefits
Relocation benefits are not available for this position
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. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants .
