¥12,000,000 - ¥16,000,000 per year, 年収1,200 ~ 1,600万円
社名社名非公開職種薬事、メディカルライティング業務内容Position ResponsibilitiesAccountable for the clinical contribution to the development of each indication strategy, including registrational and non-registrational studies, with the support of the CTPs within the asset and/or indicationAccountable for the design, execution, and analyses of each studyAccountable for clinical content for CSRs and regulatory documents (e.g., briefing books submission documents and regulatory response
社名社名非公開職種薬事、メディカルライティング業務内容Position ResponsibilitiesAccountable for the clinical contribution to the development of each indication strategy, including registrational and non-registrational studies, with the support of the CTPs within the asset and/or indicationAccountable for the design, execution, and analyses of each studyAccountable for clinical content for CSRs and regulatory documents (e.g., briefing books submission documents and regulatory response
¥10,000,000 - ¥15,000,000 per year, 年収1,000 ~ 1,500万円
社名社名非公開職種アプリケーションスペシャリスト、クリニカルスペシャリスト業務内容- 開発対象疾患のトップ医師とネットワーキングすることができる。- XXXの開発品対象の疾患領域におけるナレッジやスキルが広がる・深まる。- 医学的見地から臨床試験をサポートするため、Globalの試験責任者とネットワーキングできる。- Globalの開発・試験計画を立てる役割(Clinical Research Director)になることもできる。- 日本における承認申請をリードするプロジェクトリーダーになれる- 治験の実施可能性を世界レベルで評価する担当者にもなれる。Medical Advisors provide medical and scientific expertise and guidance to investigators and CSU (Clinical Study Unit staff performing clinical trials within a CSU cluster to ensure
社名社名非公開職種アプリケーションスペシャリスト、クリニカルスペシャリスト業務内容- 開発対象疾患のトップ医師とネットワーキングすることができる。- XXXの開発品対象の疾患領域におけるナレッジやスキルが広がる・深まる。- 医学的見地から臨床試験をサポートするため、Globalの試験責任者とネットワーキングできる。- Globalの開発・試験計画を立てる役割(Clinical Research Director)になることもできる。- 日本における承認申請をリードするプロジェクトリーダーになれる- 治験の実施可能性を世界レベルで評価する担当者にもなれる。Medical Advisors provide medical and scientific expertise and guidance to investigators and CSU (Clinical Study Unit staff performing clinical trials within a CSU cluster to ensure
¥18,000,000 - ¥23,000,000 per year, 年収1,800 ~ 2,300万円
社名社名非公開職種薬事、メディカルライティング業務内容Responsible for planning and executing medical activities and make sure timely and effective execution aligned to medical strategy. Reporting to TA Medical head1. Key accountabilities1-1. Lead Medical Strategy■ Lead and monitor the execution of the Japan Medical Plan to ensure on-time and on-budget delivery of all tactical activities or deliverables■ Provide medical and technical input into medically accurate development of Brand
社名社名非公開職種薬事、メディカルライティング業務内容Responsible for planning and executing medical activities and make sure timely and effective execution aligned to medical strategy. Reporting to TA Medical head1. Key accountabilities1-1. Lead Medical Strategy■ Lead and monitor the execution of the Japan Medical Plan to ensure on-time and on-budget delivery of all tactical activities or deliverables■ Provide medical and technical input into medically accurate development of Brand
社名社名非公開職種薬事、メディカルライティング業務内容Join a global leader in scientific research dedicated to making the world healthier, cleaner, and safer.Contribute to a world-class team at the forefront of medical device and diagnostic technology innovation.Gain exposure to diverse regulatory challenges across multiple product lines, including medical devices, in vitro diagnostics, and animal health products.求められる経験Required Experience & Skills:● Experience in RA/QA within the p
社名社名非公開職種薬事、メディカルライティング業務内容Join a global leader in scientific research dedicated to making the world healthier, cleaner, and safer.Contribute to a world-class team at the forefront of medical device and diagnostic technology innovation.Gain exposure to diverse regulatory challenges across multiple product lines, including medical devices, in vitro diagnostics, and animal health products.求められる経験Required Experience & Skills:● Experience in RA/QA within the p
¥10,000,000 - ¥13,000,000 per year, 年収1,000 ~ 1,300万円
社名社名非公開職種安全性管理、品質保証、品質管理業務内容Have a direct impact on patient health & wellbeing.Emphasize employee growth & development.Work within a global facing environment.求められる経験Experience & Skills:● 5+ years of GVP experience in medical device industry, preferably with Class IV devices.● 2+ years of management experience.● Experience interacting with key regulatory agencies like MHLW, PMDA, and TMG.● Proven ability to handle government and certification body inspecti
社名社名非公開職種安全性管理、品質保証、品質管理業務内容Have a direct impact on patient health & wellbeing.Emphasize employee growth & development.Work within a global facing environment.求められる経験Experience & Skills:● 5+ years of GVP experience in medical device industry, preferably with Class IV devices.● 2+ years of management experience.● Experience interacting with key regulatory agencies like MHLW, PMDA, and TMG.● Proven ability to handle government and certification body inspecti
¥7,000,000 - ¥13,000,000 per year, 年収700 ~ 1,300万円
社名社名非公開職種安全性管理、品質保証、品質管理業務内容Join a dynamic team dedicated to advancing healthcare through innovative quality assurance practices.Work in a collaborative environment with opportunities for professional growth and development.Contribute to the development and maintenance of cutting-edge medical devices and diagnostics that make a difference in people's lives.求められる経験Required Qualifications and Experience:● Educational background or experience meeting the requ
社名社名非公開職種安全性管理、品質保証、品質管理業務内容Join a dynamic team dedicated to advancing healthcare through innovative quality assurance practices.Work in a collaborative environment with opportunities for professional growth and development.Contribute to the development and maintenance of cutting-edge medical devices and diagnostics that make a difference in people's lives.求められる経験Required Qualifications and Experience:● Educational background or experience meeting the requ