Clinical Trials Jobs in Japan

職務内容スタディマネジャーは日本国内において治験の管理監督を担いCROや治験実施医療機関と連携しながら治験参加者の安全と福祉治験の品質を確保し治験の計画通りの実施をリードしますグローバルローカル双方と連携し課題解決や進捗管理も担当しますJOB SUMMARY & RESPONSIBILITIESResponsible for in country study/site...

職務概要臨床試験のデザイン分析解釈を関連する薬事規制要件標準業務手順書SOPおよびベストプラクティスに従って業務を行う臨床開発チームの中で特に臨床開発リーダー臨床薬理担当者統計担当者で効果的に協働し科学に基づいた統計の専門知識を生かし医薬品開発に貢献する職務内容試験デザイン統計解析計画統計解析結果の解...

JOB POSITION PURPOSEActs as a line manager leading a team of MAS. Shapes the local strategy and ensures the delivery of scientific-medical expertise and exchange with KOLs in the assigned therapeutic area with a particular focus on the designated products through a team of MAS.Lead the Pfizer Japan...

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...

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...

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...

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...

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...

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...

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...

Job OverviewThe MSL role is field based customer facing role activities should be Key medical expert (KME) focused with the intent to maximize medical one on one interactions with HCPs. Over70% field-related activities (face to face and virtual) is expected in the roleActs as a scientific expert kno...

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...