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 ...

Clinical research associate job involves site management, monitoring clinical studies, preparing project plans, ensuring subject protection and data integrity. Strong understanding of ICH GCP guidelines and local regulatory requirements required. · ...

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 ...

The Associate Director will provide leadership and guidance to CQA Program Managers and partner with key stakeholders for clinical development activities. · ...

Clinical research associate position at Medpace offers opportunity to join growing team in drug and medical device development. · ...

A Clinical Site Manager II (CSM II) serves as the primary contact point between the Sponsor and the Investigational Site. The Site Manager will manage the site/sponsor relationship as it relates to clinical trial delivery through consistent communication and support. · ...

We're seeking a Site Specialist II to support preparation of regulatory documents, · tracking of study site activation tasks in accordance with ICON SOPs/WPs, · sponsor SOPs applicable regulations/guidelines ICH/GCP. · Work with Site Partners internal key stakeholders optimize st ...

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 ...

We are looking for a Field Service Engineer to be in charge of maintenance, inspection and repair of dental treatment machines in dental clinics based in Osaka. · As a Field Service Engineer, · You will be responsible for customers in the Osaka area. · There will be business trav ...

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 ...

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 ...

Job summaryRegulatory Submissions Manager · We are currently seeking a full-time Regulatory Submissions Manager to join our Clinical Operations team in soon to be opened office in Osaka, Japan. · ...

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 · ...

Support preparation process tracking of regulatory documents site level critical documents site activation tasks in accordance with ICON SOPs/WPs Sponsor SOPs applicable regulations guidelines ICH/GCP Embrace contribute ICON culture quality process improvement focus enhancing pro ...

ICON 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. · We're looking for ...

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. ...

We're helping change how the world prevents detects guides treatment for cancer. We give patients clinicians clarity needed to make confident decisions when they matter most. · ...