69 English-speaking jobs in Créteil

Senior Development Medical Director (DMD) for Rare Neurometabolic Cluster. Leads clinical development plans and strategies for rare inherited disorders. Provides medical expertise for clinical studies from early phases to lifecycle management programs. Collaborates with cross-functional teams and external stakeholders. Requires MD degree, fluency in English, and 4+ years of clinical development experience.

Database Administrator will maintain operational status of databases, analyze and optimize performance, and contribute to business and technical projects. Requires 7+ years of experience with Oracle RAC, SQL Server, Oracle Exadata, Windows, Unix/Linux, scripting, and query languages.

Leads EMEA Professional Solutions distribution strategy for a top luxury brand portfolio, managing brand guidelines and regional initiatives. Manages business performance, monitors results, and partners with brands and channels to develop and implement projects. Requires a Master's degree, 7+ years of experience in marketing, brand management, and selective luxury distribution, and fluency in English.

Internship for 6 months in the GMO Department - Back Office Fixed Income & Commodities Vanilla. Tasks include following projects, developing macros, tracking operations, and reconciliation.

Internship within the Global Securities Settlement department. Tasks include ensuring legal documentation conformity, enriching and validating operations, monitoring transaction settlements, and resolving disagreements with counterparties.

This 6-month internship in Valuation Risk – Credit & XVA supports the FairVA/PVA calibration, monitors IPV calculations, and contributes to observability and backtesting studies. The role also involves data extraction, machine learning model design, and market data structuring.

Senior Development Medical Director (DMD) will lead clinical development plans and strategies for rare neurometabolic indications. Responsibilities include developing study protocols, collaborating with cross-functional teams, and ensuring regulatory compliance. The DMD will also provide medical expertise to clinical trials, analyze data, and contribute to publications.

Contribute to the evolution of applications for risk monitoring, including sensitivity analysis, FRTB Standard calculations, and exposure management. Develop, test, and document solutions using ActiveViam, Java, and React JS. Participate in maintaining production quality and managing application incidents.

Principal Statistician needed for global clinical trials. Responsibilities include statistical analysis, protocol development, and team leadership. Requires expertise in SAS programming, CDISC ADaM, and relevant regulations.