RVA Specialist

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 PositionA 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.This role is in Early Development Biometrics (EDB), a core function within Product Development Data Sciences (PDD) that provides strategic leadership and scientific rigor across early clinical development at Roche. We partner across Biostatistics, Analytical Data Science, and Data Management to enable data-driven decision-making from first-in-human through proof-of-concept studies.As trusted partners in early development, we design efficient and innovative clinical trials, apply rigorous statistical methods, and implement high-quality programming and analytical solutions to accelerate timelines, de-risk development, and increase the probability of technical success. Our integrated teams operate with agility and scientific depth, supporting exploratory analyses, early regulatory engagements, and complex data-generation needs across therapeutic areas. Together, we bring scientific rigor, technical innovation, and strategic insight to shape the future of early development and deliver better outcomes for patients.Early Development Biometrics is also home to Methods Collaboration & Outreach (MCO), which enables the most impactful use of quantitative methodology across PDD through internal consultation, external collaboration, and continuous capability building; and Visual Analytics, which creates and maintains interactive dashboards that drive high-quality Medical Data Review (MDR) and safety signal detection, aligned with Risk-Based Quality Management (RBQM) principles and Critical-to-Quality (CtQ) endpoints.

• The Opportunity :
• The Real-time Visual Analytics Specialist in Early Development Biometrics is responsible for designing, delivering, and maintaining interactive, study-level data visualizations that support Medical Data Review (MDR) and safety signal detection. Operating at the intersection of data science, clinical research, and digital enablement, this role ensures that visual analytics are aligned with Risk-Based Quality Management (RBQM) principles, defined Critical to Quality (CtQ) factors, and Medical Data Review Plans (MDRPs).As a Real-time Visual Analytics Specialist, you will create standardized yet customizable data visualization templates and provide study teams with high-impact graphical tools to support early development decision-making. You will also serve as a partner and point of support for clinical scientists, offering training and ongoing consultation to ensure effective use of visual analytics in study workflows. With an eye toward scalability, compliance, and scientific relevance, the Real-time Visual Analytics Specialist plays a critical role in accelerating insight generation across exploratory and safety-critical endpoints.
• You create and maintain standardized data visualizations to support Medical Data Review and safety signal detection, following established templates and guidance
• You apply defined visualization standards to generate outputs aligned with Risk-Based Quality Management (RBQM) principles and Critical to Quality (CtQ) endpoints
• You work under guidance to implement visual analytics within timelines tied to First Patient In (FPI) or predefined safety milestones
• You support documentation and quality control of visualization deliverables to ensure traceability and compliance
• You participate in training sessions and incorporate feedback from more experienced Real-time Visual Analytics Specialists
• You assist in responding to basic stakeholder requests and clarifying data availability or visualization functionality
• You work under general supervision and apply independent judgment to interpret guidance, prioritize responsibilities, and make decisions in situations that require contextual understanding
• You apply judgment to address moderately complex statistical or data issues, balancing scientific rigor with appropriate flexibility, and seek guidance when facing novel or ambiguous situations
• You adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological and regulatory expertise
• Who You Are :
• You hold a Bachelor’s degree in life sciences, computer science, data science, bioinformatics, or a related field
• You have 1-3 years of experience in clinical data, visualization, or analytics; or an advanced degree with 1-3 years of equivalent work experience
• You are familiar with tools such as R Shiny & Git, or similar platforms
• You are familiar with programming language (such as, but not limited to, R and the tidyverse)
• You have a basic understanding of clinical trial data and common data structures (e.g., CRF data)
• You demonstrate strong attention to detail, logical thinking, and an eagerness to learn visualization standards and clinical workflows
• You show respect for cultural differences when interacting with colleagues in the global workplace
• You communicate effectively in English, both in writing and verbally
• Preferred Qualifications :
• Exposure to clinical or safety data structures and terminology (e.g., adverse events, lab results, dosing)
• Familiarity with Risk-Based Quality Management (RBQM) concepts and their role in early development
• Interest in visual storytelling and user experience in data interpretation
• Ability to follow visual design templates and apply style consistency
• Curiosity and willingness to learn visualization standards and workflows in a regulated environmentRelocation benefits are not available for this posting#PDDT#PDDMissThe expected salary range for this position based on the primary location of Mississauga is 89,256.00 and 117,148.50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.We use artificial intelligence to screen, assess or select applicants for this role.This posting is for an existing vacancy at Hoffmann-La Roche Ltd.### Who we areA 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.

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