As a Project Lead in Cronos Study Operations, you will play a pivotal role in accelerating clinical trial delivery, helping bring new treatments to patients faster. · Lead or support bid defense presentations, especially for smaller or regional studies. · Manage delivery of regio ...

Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and Pfizer standards. · Res ...

This role has been designed as 'Hybrid' with an expectation that you will work on average 2 days per week from an HPE office. The job involves managing a team, leading projects, and ensuring the quality of IT services. The ideal candidate will have experience in IT project manage ...

For studies, ensure the set up and the progress of the clinical studies under responsibility, in accordance with local regulations, Good Clinical Practices, internal procedures, technical protocols. · Support the Japanese development strategy to the Core Team/Asset Team · Conduct ...

This role has been designed as ''Onsite' with an expectation that you will primarily work from an HPE office Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. · We help companies connect protect analyze act on their data applic ...

This role has been designed as 'Hybrid' with an expectation that you will work on average 2 days per week from an HPE office. As Operation Project Manager, you will be responsible for managing a team of project members, overseeing the delivery of IT services to customers, and mai ...

This role has been designed as 'Hybrid' with an expectation that you will work on average 2 days per week from an HPE office. Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. We help companies connect, protect, analyze, and ac ...

This role has been designed as 'Hybrid' with an expectation that you will work on average 2 days per week from an HPE office. · Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. · We help companies connect, protect, analyze, an ...

This role has been designed as 'Hybrid' with an expectation that you will work on average 2 days per week from an HPE office. Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. We help companies connect, protect, analyze, and ac ...

For studies, ensure the set up and the progress of the clinical studies under responsibility, in accordance with local regulations, Good Clinical Practices, internal procedures, technical protocols. · Conduct, arrange and provide the documents for the PMDA consultation in collabo ...

As a Project Lead in Cronos Study Operations, you will play a pivotal role in accelerating clinical trial delivery, helping bring new treatments to patients faster. You'll be part of a core project team responsible for executing clinical studies in alignment with contractual obli ...

The GCDSE provides clinical and R&D expertise, guidance and direction in the context of the region/country, in which they operate. · As the leader of the Clinical (or Extended Clinical) Team, the GCDSE is the clinical representative in global project teams (GPT). The GCDSE is a s ...

Rakuten is one of the world's leading e-commerce companies. We are looking for a proactive mindset who can pursue new challenges and contribute to the business by maximizing the capabilities of SalesForce. · Support the Rakuten Group's internal SalesForce implementation and custo ...

Successful project management requires that Project Managers develop strong working relationships with the client and key internal customers and organize and build effective project teams for each study. · Coordinating the project 'kick off' stage with the client in order to chec ...

Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and Pfizer standards. · Pro ...

Japan Study Manager responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and Pfi ...

We are seeking a strategic and experienced Head of Design to lead the planning, design, and delivery of the next data center projects in Japan. This individual will play a critical leadership role in scaling our local infrastructure footprint, ensuring projects are delivered on t ...

Lead the planning and design of retail store layouts in alignment with brand guidelines and customer needs. · Collaborate with internal teams and external vendors to ensure timely project completion. · Oversee budgeting, scheduling, and resource allocation for store development p ...

Facility Operations Manager to join our team at our Tokyo, Japan location. · Collaborate with internal/external stakeholders to define data center operations and develop Change Management procedures and tools. · Technical leader managing team and consultants to implement the data ...

The Clinical Research Associate II will be responsible for site management, conducting site monitoring responsibilities, and preparing project plans related to clinical monitoring. The ideal candidate will have a thorough understanding of ICH GCP Guidelines and local regulatory r ...

Health, Safety, Security, and Environment (HSSE) Manager for Integrated Management and Analytics Group. The role involves developing, revise/update, overseeing and implementing various aspects of HSSE management System within the organization, projects and operation. · ...