Quick overview
SeniorityMid Senior
Work modeHybrid
LocationSouth San Francisco, CA, United States
Clinical TrialsComplianceConcreteLLMPharmacovigilanceRisk ManagementMachine LearningAgile
Job description
Job Title: US_Data Analyst_Research I_CO
Job Location: South San Francisco California 94080
Job Duration: 12 months with possible ext
Position Summary
We are seeking a contractor with a background combining AI rapid prototyping and Predictive Modeling to support the DAISAE platform and predictive analytics subteams within the RDE 9 program. This role focuses on co-developing shared data and technical foundations (e.g. Ontologies, Knowledge Graphs), prototyping agentic AI capabilities, and advancing predictive models for drug safety risk prediction across the product lifecycle.
Key Responsibilities
Education
MSc or PhD in Data Science, Computer Science, Computational Biology, Bioinformatics, Biostatistics, Epidemiology, or a related quantitative field.
Technical Expertise
Background in pharmacovigilance, drug safety, toxicology, or quantitative risk management is highly desirable.
Soft Skills
Job Location: South San Francisco California 94080
Job Duration: 12 months with possible ext
Position Summary
We are seeking a contractor with a background combining AI rapid prototyping and Predictive Modeling to support the DAISAE platform and predictive analytics subteams within the RDE 9 program. This role focuses on co-developing shared data and technical foundations (e.g. Ontologies, Knowledge Graphs), prototyping agentic AI capabilities, and advancing predictive models for drug safety risk prediction across the product lifecycle.
Key Responsibilities
- AI Prototyping & MCP Tool Development: Rapidly explore, evaluate, and prototype emerging AI tools and agentic capabilities, specifically developing MCP tools and AI agent integrations for DAISAE.
- Predictive Modeling: Build and refine predictive models using multi-modal datasets (including in vitro, in vivo, omics, clinical trial data, real-world data (RWD), and spontaneous safety reports) to enable risk prediction from early molecule-level evaluation to late-stage and post-marketing patient safety.
- Architecture & Platform Design: Translate feasibility findings and prototype evaluations into concrete architectural design and platform requirements for shared data and technical foundations.
- Co-Development & Governance Collaboration: Work in an agile way to prototype reusable technical capabilities before transitioning components to RDT (Roche Digital Tech) for formal validation, compliance, and production rollout.
- Cross-Functional Alignment: Collaborate with data scientists, safety scientists, and RDT technical partners to ensure technical execution aligns with business priorities.
Education
MSc or PhD in Data Science, Computer Science, Computational Biology, Bioinformatics, Biostatistics, Epidemiology, or a related quantitative field.
Technical Expertise
- Strong expertise in predictive modeling, machine learning, and AI prototyping.
- Hands-on experience developing agentic AI systems, LLM tools, and MCP tools.
- Proficiency in handling biomedical datasets (omics, clinical trials, RWD, or in vitro/in vivo data).
- Agile prototyping mindset with software engineering skills tailored for data science.
Background in pharmacovigilance, drug safety, toxicology, or quantitative risk management is highly desirable.
Soft Skills
- "AI native" approach to problem-solving with adaptability to fast-moving frameworks.
- Proactive attitude and strong communication skills suitable for global matrix team settings.
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