PrimeVigilance( Ergomed Group傘下)は、医薬品安全性に特化した国際的なサービスプロバイダーとして、世界各地で事業を展開しています。ヨーロッパ・北米・アジアに拠点を構え、高品質なサービスを提供しています。 · ...

PrimeVigilanceは、医薬品安全性に特化した国際的なサービスプロバイダーです。世界各地で事業を展開しており、メディカルインフォメーション、ファーマコヴィジランス、薬事など、高品質なサービスを提供しています。 · ...

Are you ready to accelerate your potential and make a real difference within life sciences, · diagnostics and biotechnology? · ...

Design analyze and interpret clinical trials/post marketing surveillance PMS in compliance with relevant regulatory requirements company standards and best practices Provide scientifically rigorous statistical expertise and contributions by working effectively within the clinical ...

We are seeking a highly motivated Regulatory Affairs Manager to lead regulatory strategies and ensure compliance for pharmaceutical and medical device products. This role plays a critical part in supporting product launches, ...

This role is responsible for ensuring optimal patient safety by developing a state-of-the-art safety strategy. · Develop and maintain local safety assurance system. · Conduct self-inspection and support internal process audits. · ...

We are expanding our sales team to accelerate product penetration through appropriate information delivery to healthcare professionals and strategic area-based activities. · ...

We are a leading Global CRO Company providing drug discovery development lifecycle management and laboratory services. · We provide tailored solutions to ensure safety efficacy of clients' needs focused on compliance with strict regulations. · Clinical Trial Monitoring for Phase ...

Medical Representatives provide medical information to healthcare professionals about our medicinal products. · Collecting data on used medicines from healthcare professionals and reporting it back. · Maintaining accurate records of medication use in pharmacies. · ...

Medical Representatives provide medical information to healthcare professionals about our pharmaceutical products. · The role involves providing accurate information about our products' effectiveness and safety to ensure appropriate use by patients.Collecting feedback from health ...

Medical Representatives provide information about medicines to healthcare professionals in order to promote their appropriate use. · Collects information on medicine usage at healthcare sites. · Reports on effectiveness and safety of medicines used by patients. · ...

MR(Medical Representatives)とは医薬情報担当者の略称で⾃社の医療⽤医薬品を中⼼とした医薬情報(医薬品およびその関連情報)を医療関係者に提供し、 · ...

安全性情報部は、GSK Japanが販売している製品の副作用等の安全性情報を適切に入手できるよう対処し、入手した情報を管理している部署です。 Pharmacovigilance(PV/安全性)業務は、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。 · ...

The Safety Information Department is responsible for obtaining and managing safety information about GSK Japan's products. · We are looking for someone with experience in handling safety-related documents and data entry, · who can work efficiently and effectively in our team. · ...

The Pharmacovigilance department is responsible for ensuring that safety information about GSK Japan products can be obtained and managed properly. · ...

We are seeking a Principal/SAP Architect to join our team in Tokyo. As a key member of our Solution Delivery team, you will be responsible for designing and implementing SAP solutions that drive business outcomes. You will work closely with project managers, development teams, an ...

+ Field service engineer responsible for repairing maintaining installing various products including water quality analysis instruments. · + Requires domestic travel approximately 3-4 days per week English proficiency ability to read technical documents translation software prefe ...

+ Develop and maintain enterprise applications + Design and implement new features and enhancements on existing applications using .NET, Java and JavaScript technologies + Monitor troubleshoot and resolve issues in production systems to ensure stability and performance · + Condu ...

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. · ...

The CAI Japan team is looking for individuals with a variety of experience in the field of commissioning, qualification, and validation (CQV) of production facilities and equipment in the pharmaceutical/medical device/biotechnology industry. · Create CQV protocols · ...

Safety information department is responsible for collecting and managing safety information of GSK Japan's products. Pharmacovigilance (PV/safety) business is an important job to protect patients' safety not only in Japan but also worldwide. · ...