4149 English-speaking jobs in Île-de-France

Expert consultant needed for Agentic Generative AI in insurance document processes. Design, configure, and optimize AI agents using the Onyx solution for document analysis, retrieval, and generation. Requires mastery of LLMs and advanced prompting.

Lead and develop a team focused on cost-efficient specialized models and AI security. Own end-to-end delivery of high-quality AI systems, balancing quality, latency, cost, and safety. Requires deep AI/ML expertise and product instinct.

Shape scientific storytelling and claims strategy at the intersection of R&D, Brand, and Digital Product. Translate complex research into credible, differentiating content while maintaining scientific accuracy.

Define and drive enterprise-wide AI architecture vision as a Solution Architect for Agentic AI. Design end-to-end solutions, define reference architecture, and drive adoption of AI best practices across products.

Director, Health Economics & Outcomes Research supports the hematologic oncology portfolio by building HEOR strategies for clinical development and market access. This role leads health economic models, HTA submissions, and RWD studies.

Financial Manager oversees budgeting, reporting, and P&L consolidation for entities. This role involves analyzing balance sheets, ensuring financial accuracy, and partnering on profitability and financial structuring. Requires 8-10 years of management control/audit experience and a Master's degree.

Senior Scientist to expand biobank by establishing patient-derived organoids from fresh surgical specimens, starting with NSCLC. Develop and optimize robust culture protocols for high-quality biological models. Requires PhD and 5+ years of hands-on experience.

Senior Research Engineer focusing on light-biology and biosignals. Requires PhD/equivalent, 3+ years post-doc in applied physics/photonics, and expertise in light characterization and biosignal acquisition (EEG, EOG). Strong Python/MATLAB skills are essential.

Lead operational planning and delivery of Ciliatech-sponsored European clinical studies. This role manages study execution, site/vendor oversight, budget, and cross-functional coordination for complex multicentre medical-device trials.

QPI Expert role requires 8+ years in Quality and Pharmacovigilance within the pharmaceutical industry. Responsibilities include managing client procedures, NC/CAPA, and training staff. Key skills involve QMS tools, ISO 9001, and client-facing defense of processes.

Senior Early Phase Statistician for Clinical Development. Provides statistical leadership for early clinical trials, including first-in-human and dose escalation. Requires 6+ years in pharma/CRO with expertise in adaptive designs and SAS/R.

Senior International Clinical PM to manage pediatric oncology clinical trials. Responsibilities include overseeing timelines, budget, and quality, managing stakeholders, and ensuring ICH-GCP compliance. Requires a Life Sciences degree and clinical project management experience.

Associate Director, Clinical & Scientific Affairs leads European clinical and scientific activities. Responsibilities include building user communities, managing advisory panels, and coordinating evidence generation for market access. Requires a PhD and 5+ years in the genomics industry.

Manage the Synthetic Biology Design & Profiling group at a private industrial biofoundry. Drive innovation by designing novel genetic pathways and microbial chassis using synthetic biology tools. Develop automated workflows for rapid prototyping and optimization.

Design and prototype few-shot imitation learning algorithms for humanoid robots. Advance state-of-the-art in imitation and policy learning using real robots. Requires PhD in robotics or ML and deep expertise in imitation learning.

Senior Scientist in Enzyme Technology drives scientific discovery and application of enzymes for product innovation. This role leads a team, manages cross-functional projects, and coordinates internal and external enzyme partnerships. PhD required.

Principal Scientist for a 6-month mission supporting Danone's global health impact agenda. Focus includes Iron Impact, DIJ 2030 KPI, strategic partnerships, and nutrition roadmap deliverables.

Laboratory Specialist responsible for preparing equipment, procedures, and ensuring lab readiness for plant start-up. Develop and implement the Laboratory Information Management System and mentor personnel. Requires a Master's in Chemical or Petroleum Engineering and 15+ years in Oil & Gas.

Senior Clinical Project Lead to design, implement, and coordinate global clinical studies. Responsibilities include protocol preparation, regulatory dossier management, and managing investigator relationships. Requires 6-8 years in clinical development, including Phase II and III.

Clinical Project Manager to design, implement, and coordinate clinical studies. Responsibilities include protocol preparation, regulatory dossier management, and managing investigator relationships. Requires 6-8 years in clinical development (Phase II/III) and international experience.