4621 English-speaking jobs in Île-de-France

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.

Lead the development and implementation of Global Clinical Data Standards to support regulatory submissions. This role requires expertise in CDISC, SDTM, and ADaM, partnering cross-functionally to optimize data collection.

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.

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.

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 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.

Senior Patient Safety Scientist for Rare Diseases. Lead global patient safety, ensuring robust surveillance and integrated safety assessments to support product safety profiles and risk management actions.

Senior Petrophysicist provides technical support for geoscience studies, resource quantification, and uncertainty reduction. Responsibilities include well data interpretation, reservoir characterization, and mentoring junior staff. Requires 10+ years of experience.

Senior Petrophysicist provides technical support for geoscience studies, well data interpretation, and reservoir characterization. Requires 10+ years of experience in petrophysics, well log interpretation, and formation evaluation.

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.

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.

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.

Senior Biostatistician authors protocol sections, proposes study design, calculates sample size, and performs statistical analysis using SAS. Responsibilities include authoring analysis plans, reviewing CRFs, and providing statistical consultancy. Requires a Ph.D. in Statistics or equivalent with relevant industry experience.

Senior Staff Research Scientist and Team Lead to develop and lead impact-driven projects in frontier AI, including language, speech, and computer vision models. Requires 10+ years of experience and a strong publication record.

Senior Research Scientist & Team Lead to drive impact-driven projects in frontier AI. Lead research, set roadmaps, and mentor teams in areas like language, speech, and computer vision. Requires 10+ years of experience and a strong publication record.

Architect the growth engine by defining and executing the go-to-market strategy. Oversee Growth, Revenue Ops, and Sales Enablement, managing acquisition campaigns and developing teams. Requires 10+ years in B2B scale-ups.

Develop COA endpoint strategies and lead COA instrument development across clinical programs. Advise on regulatory interactions, including FDA engagement, and serve as a subject matter expert. Requires deep COA expertise and advanced degree preferred.

Oversee Good Clinical Practice compliance for sponsored studies. Manage deviations, CAPAs, and TMF reviews while ensuring inspection readiness. Qualify systems and embed compliance into data workflows.

Senior field-based scientific ambassador for Oncology, Immuno-Oncology, and GI malignancies. This hybrid role requires an MD, PharmD, or PhD to execute regional medical plans and engage Key Opinion Leaders.

Lead the Theory & Applications team at C12, driving the theory roadmap across hardware modeling, quantum error correction, and industrial quantum algorithms. Define scalable quantum computing architectures.