Clinical Site Associate - Office Hybrid in Tokyo Osaka at ICON plc, a world-leading healthcare intelligence and clinical research organization. · ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development ...

経営層と直接連携し、会社の成長戦略をクリニカル方面から推進 · 国内の臨床研究の一貫管理 · ステークホルダー調整・規制対応 · データ・臨床ワークフローの監督 · チーム指導 · SOP改善 · DX推進 · 理系大卒以上 · 日常会話レベルの英語力 · 日本国内試験の計画~終了までの試験管理経験 · 外部ステークホルダーとの調整経験 · データ管理・臨床オペレーション・規制対応の実務知識 · スタッフ指導・育成、SOP・OJT改善等への意欲 · PMDA対応のご経験 · ...

Deep Intelligent Pharma is pioneering the transformation of the pharmaceutical industry with a revolutionary AI-native, multi-agent platform. Our mission is to empower pharmaceutical and medtech innovators by turning regulatory and clinical complexity into a catalyst for speed, s ...

Join our growing team as a Clinical Research Associate (CRA) to conduct qualification initiation monitoring and closeout visits at research sites. · Conduct qualification initiation monitoring and closeout visits at research sites · Communication with medical site staff including ...

This position is accountable for the direct management of assigned monitoring/site management related clinical trial staff across all clinical trial types. · Accountable for the identification, onboarding, training and development of monitoring clinical trial talent to support th ...

Join our growing team as a Clinical Research Associate and receive training to become a fully functional CRA with the opportunity to work home-based. · Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; · ...

FSA-Site Contracts Negotiator negotiates and maintains clinical trial agreements, amendments, and other ancillary agreements with study sites. · ...

Project Manager, FSA role involves managing site activation, coordinating with internal teams and stakeholders, and ensuring quality standards are met. The position requires strong leadership and communication skills, with a focus on driving site activation and exceeding customer ...

Director, FSAICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development · 当社では、I ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.As a Site Management Administrator, you will be responsible for managing the operations of our facilities in ...

Join our growing team as a Clinical Research Associate and have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. · Clinical Research Associate - join our growing team · Are you a recent or upcom ...

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. · Quality check on submission documents and site essential documents; · Interaction with US Cent ...

Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCP. · Work with S ...

Medpace is a leading CRO for biotech companies, adding leaders to its Clinical Trial Management team in Japan. Clinical Trial Managers with expertise in various therapeutic areas are welcome to continue working in their area of expertise or expand to a new one. · Effective manage ...

Associate Director, GCP Compliance is responsible for directing and driving the implementation of regional compliance management related to quality events and internal audits for clinical trial delivery functions. · Direct and drive the implementation of regional compliance manag ...

Direct and drive the implementation of regional compliance management related to quality events and internal audits for clinical trial delivery functions including the identification and development of applicable processes and tools. · Direct and drive the implementation of regio ...

Fluent in both Japanese and English. Shapes and executes an overall marketing strategy. Communicates this strategy to the marketing team and other business units. Coordinates with sales management in order to ensure alignment of marketing and sales strategies. Evaluates past prog ...

Fluent in both Japanese and English shapes and executes an overall marketing strategy communicates this strategy to the marketing team and other business units coordinates with sales management in order to ensure alignment of marketing and sales strategies evaluates past programs ...

Be part of something altogether life-changing Working at Cytiva means being at the forefront of providing new solutions to transform human health Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccin ...

Project Manager, FSA role involves managing site activation, coordinating with internal teams and stakeholders, and ensuring compliance with corporate and departmental policies. · Drive and accelerate site activation activities · Coordinate with internal teams and stakeholders · ...