Biotechnology Research Jobs in Japan
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Alexion Japansenior (labeling) Manager Regulatory
Astrazeneca
Position Summary Senior Manager Regulatory Affairs should be responsible for creating Japanese Package Inserts (JPIs; i.e. Japanese Labeling) of new drugs and manage revisions of JPIs of post approval products and review of educational materials ( with the advice of Director or Associate Director as...
Director, Regulatory Affairs
Iqvia
会社紹介ビジョン私たちIQVIAはヒューマンデータサイエンスの先駆的な企業として医療ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで誰もがより健康に自分らしく生きられる社会の実現を目指しています世界最大規模を誇る医療ヘルスケア関連データを基盤に人データサイエン...
Senior Director, Regulatory Affairs
Parexel
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...
[medtech] Associate Director, Biosurgery, Regulato...
Johnson & Johnson
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...
Regulatory Cmc Expert (manager), Japan
Csl Plasma
Position Purpose: The Regulatory CMC Expert evaluates all CMC regulatory aspects related to the assigned products (including both development products and established products) in Japan.The Regulatory CMC Expert develops and executes CMC strategies for development products/life-cycle management of e...
Senior Regulatory Affairs Consultant Cmc
Parexel
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...
Regional Medical Affairs Manager Sr. Regional Medi...
Gossamer Bio
Summary:The Regional Medical Affairs Manager / Sr Regional Medical Affairs Manager will be responsible for facilitating scientific exchange and clinical support for Gossamers clinical studies and will engage with clinical study sites investigators and study personnel to encourage fast study start up...
[innovative Medicine] R&d, Medical Writer I , Medi...
Johnson & Johnson
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...
[medtech]medical Affairs Manager-shockwave
Johnson & Johnson
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...
[innovative Medicine] R&d, Scientist, Cmc Group, C...
Johnson & Johnson
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...
Sr Manager, Medical Affairs (liver) Hybrid Msl
Gilead Sciences
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...
Principal Medical Writer
Regeneron Pharmaceuticals
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...