Clinical Development Jobs in Japan

We are looking for a passionate and experienced Senior Manager to join our Global Development Quality & Regulatory Compliance team as the Global Development Quality Lead for Japan (GDQL-J). In this key role you will lead quality and compliance initiatives within our local affiliate operations suppor...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment ap...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

Identify and secure new licensing opportunities in accordance with agreed licensor strategiesFill category/product type gaps and achieve specific revenue goals and annual growth for the territory/regionBe the primary commercial contact for your licensees and manage the day-to-day licensing business;...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

Job DescriptionSenior Account Executive Healthcare & Life SciencesHybrid TokyoWere a leader in data and AI. Through our software and services we inspire customers around the world to transform data into intelligence - and questions into answers.If youre looking for a dynamic fulfilling career with...

ABOUT THE ROLE日本におけるホテルポートフォリオの拡大をリードする開発ディレクターを募集しています本ポジションはAccorの全ブランドを対象にさまざまな契約形態運営受託フランチャイズレジデンスやプロジェクトタイプホテルリゾート長期滞在型ブランドレジデンス複合開発に関する開発案件の獲得交渉契約締結までを担う...

We are a global team of innovators and pioneers dedicated to shaping the future of observability. At New Relic we build an intelligent platform that empowers companies to thrive in an AI-first world by giving them unparalleled insight into their complex systems. As we continue to expand our global f...

Job DescriptionPOSITION OVERVIEW:The Associate Director of the Regulatory Affairs (RA) is responsible for the management of regulatory affairs activities including pharmacovigilance work at RA department at PDRA division of Animal Health in Japan. The position requires a combination of scientific kn...

Work Flexibility: Hybrid or OnsiteAbout the job:The role exists to oversee entire Medical Business Unit and drive the team to ensure the attainment of financial and operational goals in support of Stryker Japans overall financial and strategic objectives. The position holder will plan direct and coo...

Position OverviewOur mission is to safeguard patient safety and lead pharmacovigilance (PV) in Japan.The Senior Manager Global Patient Safety (GPS) reports to the Director GPS (Safety Management Officer) in Japan and serves as a core leader for safety operations overseeing the handling of Individual...

Job ScopeContribute as a medical writer with primary expertise in clinical documentation while also supporting nonclinical sections as needed. This role leads and supports the development of regulatory documentsincluding CTD modules and briefing documentsand actively participates in strategic regula...

We are seeking an experienced and detail-oriented Manager Regulatory Submission Project Management (RSPM) to join our dynamic team. This pivotal role offers the opportunity to lead the planning execution and review of regulatory operations activities ensuring the successful submission of regulatory...

We are seeking an experienced and detail-oriented Manager Regulatory Submission Project Management (RSPM) to join our dynamic team. This pivotal role offers the opportunity to lead the planning execution and review of regulatory operations activities ensuring the successful submission of regulatory...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

The Creative team provides customers with original relevantand contemporary industry-uniquecombination of consumer research proprietarydataandthree decades oftrendreportingexperience the teamdeliversactionableinsightsthatguidecustomersto the visual content that connects with consumers. Closelycolla...