Clinical Site Manager II

. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study... lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory...

Lugar: Tokyo | 03/04/2026 02:04:51 AM | Salario: S/. No Especificado | Empresa: ICON

Senior Clinical Trial Associate

with study protocols and regulatory requirements. Collaborating with cross-functional teams to support trial operations... and resolve any issues that arise during the course of the study. Monitoring and tracking trial progress, including managing site...

Lugar: Osaka, Osaka | 03/04/2026 00:04:18 AM | Salario: S/. No Especificado | Empresa: ICON

Clinical Site Manager II

success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.... What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical...

Lugar: Tokyo | 03/04/2026 00:04:52 AM | Salario: S/. No Especificado | Empresa: ICON

Business Operations Associate - Site and SSU Specialist

, and we welcome you to join us on our mission to shape the future of clinical development Job Advert Posting We are currently seeking a Study Start Up Associate... II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role...

Lugar: Tokyo | 02/04/2026 18:04:21 PM | Salario: S/. No Especificado | Empresa: ICON

Senior Medical Writer

and therapies. What you will be doing Leading the preparation, review, and editing of clinical study documents, including... clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring...

Lugar: Tokyo | 02/04/2026 18:04:54 PM | Salario: S/. No Especificado | Empresa: ICON

Clinical Site Manager II

success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.... What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical...

Lugar: Tokyo | 02/04/2026 17:04:50 PM | Salario: S/. No Especificado | Empresa: ICON

R&D Study Operation General & Specialty Medicine/IDs & Vaccines CRM

. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift...む臨床開発の実務経験(目安:5年以上) 臨床試験オペレーションへの高い関心と、将来的にCRMとして成長していく意欲 チーム内外の関係者と協働できる高い対面コミュニケーション能力 CRM、Study Manager、CROにおけるProject...

Lugar: Chiyoda, Tokyo | 02/04/2026 01:04:46 AM | Salario: S/. No Especificado | Empresa: MSD

General Manager

welcomes international students year-round to study Japanese language and culture in one of the world's most dynamic cities..., travel, cultural exchange, and academics-turn dreams into international opportunities. When you join EF...

Lugar: Tokyo | 31/03/2026 17:03:54 PM | Salario: S/. No Especificado | Empresa: EF Education First

Medical Advisor, Rare Liver Diseases

landscape. The Medical Advisor will work closely with other Ipsen personnel to ensure scientific and technical needs... of Medical Affairs, Clinical Development and commercial colleagues are identified and met. He/she will also work with cross...

Lugar: Tokyo | 30/03/2026 22:03:50 PM | Salario: S/. No Especificado | Empresa: Ipsen