Facility Safety Jobs in Tokyo

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

As People Relations Manager you have complete responsibility and accountability for the People Relations areas for the countries in scope. E.g. implementation of global deliveries and processes policies and guidelines securing that local laws practices and needs are captured and cater More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

The Japan Graduate Development Programme (GDP) is a competency framework which supports development needs highlights experience gaps enhances knowledge and gains firsthand experience for graduates. The GDP will run for approximately 24 months starting in April 2026 Graduate Devel More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

As a Regulatory Officer will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities deliver regulatory training to project teams and communicate with stakeholders on regulatoryrelated matters. Join PSI and help drive innovation a More...

Were searching for a knowledgeable teamoriented CRA II to manage the clinical aspects of fullservice global projects in Japan. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical re More...

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to More...

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to More...

Were searching for a knowledgeable teamoriented CRA II to manage the clinical aspects of fullservice global projects in Japan. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical re More...