· 英語も活かせる医薬文献の検索・/週2在宅OK · 藥学知識が活かせるお仕事/日本語・英語の医薬論文検索+社内対応在宅勤務もありで働きやすさ抜群 · · 大手企業のシェアード会社/メディカル部門でのお仕事です 時給2100円の高時給医療製薬業界での経験を活かせる 【おすすめPOINT】 醫药文献的检索 · 调查工作是主要业务，简单，可以集中 · 英语论文的检索存在（可以使用翻译工具）/英语技能也可以发挥作用 · ...

We are seeking a RegulatoryAffairs Specialist to join our team at JohnsonandJohnson.The successful candidate will be responsible for maintainingand managing regulatory approvals for pharmaceutical products including surgical suturesand adhesives. · ...

+ · The company seeks an experienced professional for its regulatory affairs team responsible for maintaining management of Japan general surgery field products including sutures tissue adhesives etc. ...

+This role involves maintaining regulatory approvals for general surgery products including sutures and tissue adhesives. · +Promptly managing regulatory compliance activities across various regions. · Establishing strong relationships with key stakeholders within local authoriti ...

The position involves proposal sales of reagents and equipment for clinical laboratories at medical institutions, focusing on biochemical and immunological assays. The successful candidate will build relationships with hospital administrators and laboratory technicians, identifyi ...

This position is responsible for conducting scientific evaluations of drug characteristics from a non-clinical perspective, developing domestic development strategies, and preparing materials to meet regulatory requirements. It also contributes to the implementation and approval ...

Clinical Research Specialist role involves leading clinical trials planning and execution in collaboration with various departments. The specialist will be responsible for creating or reviewing related documents such as SOPs and managing trial milestones. · ...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. · ...

Servier is committed to therapeutic progress for patients benefit. · Work within Servier Group helps advance therapeutic progress. · ...

+ Job summary · As a Customer Quality Specialist at Johnson & Johnson, you will be responsible for ensuring the quality of our products and services. You will work closely with internal departments and external stakeholders to resolve customer complaints and improve product quali ...

Nonclinica Project Specialist job description and requirements in Japan. · ...

PMS and pharmacovigilance are important jobs to protect patients' safety in Japan and around the world. Our business is to collect, evaluate, and implement appropriate measures for post-marketing information on our products while following laws. · ...

Job summary: The Safety Control Associate is responsible for ensuring compliance with regulatory requirements in Japan. They will coordinate safety control activities such as pharmacovigilance (PV) monitoring, risk management planning (RMP), and third-party audits. Key skills inc ...

PMS (Pharmacovigilance) is an important function that ensures patient safety worldwide under strict regulations. · ...

The company is seeking a Quality Assurance Technical Service Specialist for their Tokyo office. The successful candidate will be responsible for managing quality control processes, collaborating with external partners, and ensuring compliance with regulatory requirements. · Manag ...

We believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, · `Plan, prepare and execute necessary regulatory actions to support business objectives. · `}`Company's business strategy ...

At Johnson & Johnson, · We believe health is everything. · Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,treated,and cured, · where treatments are smarter and less invasive, · and solutions are personal. · ...

+ Job summary: At Johnson & Johnson we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured. · + Qualifications:At least 5 years of pharmaceutical business experience with medical d ...

We are seeking an Associate Consultant (PRO) to join our team at IQVIA Japan. · Conduct Outcome Research to generate evidence in healthcare and public health domains. · Design and implement diverse research methodologies. · ...

PMSやPharmacovigilance(PV/安全性)は、患者さんの安全を守る重要な仕事であり、日本だけでなく世界各国で厳しい法規制が設けられています。我々の業務は、これら法規制を守りながら、自社製品の市販後の有効性や安全性の情報を収集、評価し、適切な対策を実施することです。また、昨今、様々な会社と提携したり、これまでとは異なるデータやAIなども活用してビジネスを行う必要性も増しており、このような環境変化にも対応しながら、上記の業務を適切に実施する必要があります。 · ...

We are seeking a Senior Consolidated Accounting Officer to join our team. The successful candidate will be responsible for preparing consolidated financial statements, reviewing and reconciling accounts, and performing other accounting tasks as required. · Create and review conso ...