The Regulatory Affairs TA will be responsible for ensuring first time approval of new products and new indications for existing products through participation in local brand teams. · ...

The Head of Regulatory Affairs in Japan will act as the representative of the regulatory affairs organization to the Japan affiliate and be a member of AbbVie Management Team in Japan. · Accountable for day-to-day management of the regulatory team in Japan. · Develop and manage J ...

Pipeline Medical Science Leads are key members of the affiliate medical department. They interact with investigators participating in our enterprise critical studies, communicate information, and facilitate scientific dialogue about AbbVie's investigational products in a strictly ...

The Japan Regulatory Strategy Group Sr Mgr is developing and executing the regulatory strategies and plans; providing strategic regulatory expertise for drug development; interfacing with regulatory authorities; aligning with key cross-functional partners; integrating into Amgen' ...

The Senior Manager, Government Affairs will report directly to the Vice President and Head of International Government Affairs for Alibaba. This newly created role will be based in Tokyo, Japan. The successful candidate will manage regulatory and political matters in Japan in are ...

The Japan Program Clinical Head (JPCH) is responsible for clinical program activities for approval and post approval commitment for Re-examination in Japan. · Lead the JCT and represent Clinical Development on the JPT to achieve valuable clinical program strategy, drive innovatio ...

The Head of Medical Therapeutic Area is responsible for leading the Medical therapeutic area team, developing medical strategy and operationalizing medical activities as a key member of the Brand Team. He/she shall engage and build strong links with key external medical experts i ...

We are looking for a Medical Science Liaison to drive TAE Management to identify develop build professional relationships with TAEs Discuss unmet medical needs treatment strategies of diseases provide them fair balanced exchange medical scientific information Educate speakers cre ...

The Head of Medical Therapeutic Area is responsible for leading the Medical therapeutic area team, developing the medical strategy/plan and operationalization of the medical activities. · Qualifications in a relevant discipline such as medical, pharmacy, biotechnology, life scien ...

The Director of RWE-HO Japan leads the local evidence strategy to demonstrate the value of GSK's innovative medicines/vaccines. This role ensures local real-world clinical, economic and humanistic evidence supports regulatory, reimbursement, and patient access objectives. · This ...

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 ...

Coordinate CMC regulatory strategy activities for assigned projects throughout development phases. Manage CMC Regulatory relationship with Global CMC to ensure alignment between Japan-Global CMC strategy. · Lead CMC regulatory strategy development for assigned projects ensuring C ...

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 ...

We are looking for a talented, innovative, and well-connected individual to represent AWS in Japan before policymakers that are strategically important to the AWS business. · Key job responsibilities include addressing policy risks to the business as well as advancing strategic b ...

This Tokyo-based Government Affairs And Public Policy Position, Which Is a Member Of Japan Public Policy Team, And Will Also Participate In The APAC Public Policy Team, · shall develop and implement advocacy strategies related to cloud adoption by the Japan public sector. ...

The R&D Specialist/Manager is responsible for leading Japanese regulatory strategy and target labeling in J-CDT, sharing information with the Global Regulatory Team (GRT), and participating in GRT meetings to provide Japanese input. ...

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Lead Japanese regulatory strategy and target labeling in J-CDT, and share the information to the Global Regulatory Team (GRT) · Princ ...

Lead Japanese regulatory strategy and target labeling in J-CDT, and share the information to the Global Regulatory Team (GRT). Prepare Common Technical Document (CTD) for Japan. Provide input on study design, conduct, and need for any additional studies for Japan. · ...

Johnson & Johnson Innovative Medicine is recruiting for a Medical Director Clinical Science Oncology. The successful candidate will oversee and ensure the flawless execution of assigned clinical studies in Japan, and contribute to the global clinical development strategy via prov ...

This job is for a Medical Director in Clinical Science Oncology at Johnson & Johnson in Tokyo, Japan. The job involves overseeing clinical studies, providing clinical leadership, and working with global teams. The ideal candidate will have an MD or PhD, experience in oncology cli ...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in ...