Regulatory Documents Jobs in Tokyo

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...

Job PurposeThe Clinical Scientist (CS) in Japan is the single point accountability for the development of the Clinical Development Plan (CDP) study design governance and interpretation of results of the studies and filing strategy and key messages in CTD (clinical modules) for Japan. The study desig...

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...

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...

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...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifePosition Title Legal Entity ControllerDIAB @...

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...

SUMMARY:The Principal Medical Writer (PMW) is the accountable lead for his/her compound(s). The PMW works closely with Medical Directors Biostatisticians Regulatory Liaisons and others to develop high-quality clinical documents and is responsible for helping to drive document strategy development an...

ECシステム開発プロジェクトリード / Tech Lead and ComplianceDescription -主に日本組織内のユーザーのニーズやビジネス要件に対応するソフトウェアアプリケーションの設計開発テストおよび保守を担当します職務は機能的でユーザーフレンドリーかつ信頼性の高いソフトウェアソリューションを作成するために国内国外の部門...

BandLevel 4Job Description Summary-Contributes with appropriate oversight to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule budget quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member o...

Job Summary:To provide specialist regulatory knowledge and support for chemicals to ensure the regulatory compliance of these materials for both internal and external customers. Learning the requirement of and supporting the CSCL regulatory business.This role contributes to departmental revenue targ...