Senior Statistician, Clinical Statistics - Tokyo, Tokyo

+Job summary · Senior Statistician will collaborate with representatives from other functions to plan studies execute analyses and report results. · +QualificationsMasters degree or above preferred · At least 6 years of experience as statistician independently (including sNDA sub ...

We are seeking new grads for Biostatistician to join our Biostatistics team in Japan. · ...

We are seeking a full-time Sr. Manager of Biostatistics in our Tokyo office. This role will lead the APAC Biostatistics team and provide leadership for solutions in data management, analysis and reporting related issues. · Manage analysis databases for clinical trial projects. · ...

We are currently seeking a full-time Sr. Manager of Biostatistics in our Tokyo office. · ...

Design analyze and interpret clinical trials/post marketing surveillance PMS in compliance with relevant regulatory requirements company standards and best practices Provide scientifically rigorous statistical expertise and contributions by working effectively within the clinical ...

Ourcorporateactivitiesaregrowingrapidly,andwecurrentlyseekingafull-timeoffice-basedStatisticalAnalysttojoinourBiostatistics teaminJapan.Thispositionwillworkontaamteamtoaccomplishtasksandprojectsthatareinstrumentaltothecompany'ssuccess. · ...

We are seeking new grads for Statistical Analyst to join our Biostatistics team in Japan. · ...

+Job Summary · +Our corporate activities are growing rapidly, and we are currently seeking a full-time office-based Statistical Scientist to join our Statistics team in Tokyo Japan. · +This position will work on a team to accomplish tasks and projects that are instrumental to the ...

Make your mark for patients by joining our Biometrics & Data Sciences department as a statistician. You will support global clinical development with innovative statistical analysis and data science methods. · ...

The Medical Writer (Director-level) will lead the development of Japan-specific regulatory documents required for submissions to Japanese regulatory authorities (PMDA/MHLW), including CTD modules, consultation briefing documents, and responses to PMDA inquiries. · ...

We are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in Tokyo or Osaka Japan This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming ba ...

We are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in Tokyo or Osaka, Japan. · ...

Senior medical writer at ICON plc leading development execution medical writing strategies clinical research projects contributing advancement innovative treatments therapies. · Leading preparation review editing clinical study documents including protocols CSRs IBs regulatory su ...

We are currently seeking a Senior Medical Writer to join our diverse and dynamic team. As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects, contributing to the advan ...

This Is What You Will Do · The Associate Director, Data Scientist will lead the development of advanced data utilization platforms that integrate and analyze diverse data from both inside and outside the organization. ...

This Is What You Will Do · The Associate Director will lead the development of advanced data utilization platforms that integrate and analyze diverse data from both inside and outside the organization. · Designing developing and deploying predictive models and machine learning al ...

The Global Clinical Development Strategy Expert (GCDSE) provides clinical and R&D expertise, · guidance and direction in the context of the region/country, in which they operate. · Clinical representative in global project teams (GPT), accountable for CDP implementation · ...

The GCDSE provides clinical and R&D expertise to move vaccine candidates through development. They lead global project teams and ensure consistency across trials in terms of site selection approval process and safety data quality review. · ...

This position will directly report to Head of Device Quality division/Facility Manager, and have a responsibility for operations for quality controls applied in the medical devices at the facility locating in Chiba prefecture in Japan. · Manage quality control activities for Raku ...

This is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow. · ...