Biostatistician

2291 Roche Molecular Systems, Inc.; Indianapolis (IN); Sur place; USD 103 000 - 190 000; Plein temps

Avantages offerts par ce poste

Discretionary annual bonus

Résumé du poste

Roche in Indianapolis, IN seeks a senior statistician to partner with clinical teams, design robust studies, write SAPs and reports, and ensure rigorous data integrity across diagnostic development.

You will mentor teammates, push methodological innovation, and share findings through publications and conferences, contributing to regulatory-ready analyses that advance Roche’s mission to improve healthcare.

Qualifications

• Master’s degree in Statistics, Biostatistics, or a closely related quantitative field with 9+ years of experience (or a PhD with 6+ years).
• Hands-on proficiency in SAS or R for statistical analyses and reporting.
• Understanding regulatory considerations for in vitro diagnostic (IVD) devices, including sensitivity, specificity, agreement rates, and reproducibility evaluations.
• Experience in collaborative, multi-disciplinary environments with cross-functional alignment and QC.
• Strong ability to communicate statistical concepts clearly to diverse scientific audiences via presentations or publications.

Responsabilités

• Design robust clinical studies and select sound statistical methodologies.
• Write SAPs and detailed statistical reports for health authority review and scientific evaluation.
• Perform end-to-end data analyses, coordinate sample randomization and blinding, and supervise QC processes.
• Develop novel statistical solutions and study design improvements for diagnostic development.
• Mentor team members and share knowledge through publications, conferences, and cross-functional workshops.

Connaissances

Statistics

Biostatistics

Communication

Team collaboration

Formation

Master’s degree in Statistics or Biostatistics

PhD in Statistics or related field

Outils

SAS

R

Description du poste

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 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.

Compensation and Benefits

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.

Our Culture & Values

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. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche.

Equal Opportunity Employer

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.

Accommodations for Applicants

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.