The Medical Information Manager will be responsible for contributing to team objectives while supporting and collaborating with team members. · Complete tasks along with the team objectives. · Support and collaborate with team members. · ...

The Medical Information Specialist will collect medical/scientific information regarding company products and respond promptly to inquiries and requests from internal and external stakeholders. · ...

The Medical Manager will be responsible for planning and executing medical activities and ensuring timely and effective execution aligned to medical strategy. · ...

· Medical & scientific subject matter expert for assigned Disease Area (eg: dermatology, rheumatology) Generate medical and scientific evidence to fulfill unmet medical needs through utilization of RWD/RWE Transversally collaborate with other functions locally and globally to he ...

Promote products to patients in designated areas, contributing to patient outcomes. Develop territory strategies based on PVS and achieve sales plans while collaborating with partner companies. · ...

Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients. · Acts as a field-based expert, building relationships with External Experts as trusted scientific partners. Exchanges credible ...

The Medical Science Liaison (MSL) role involves exhibiting scientific and clinical knowledge to facilitate timely and appropriate exchanges with influential external experts. · Exhibits strong knowledge of relevant diseases, healthcare environment, competitors; can articulate med ...

The Japan Sr Project Lead serves as the project leader for development pipelines with comprehensive responsibilities including end-to-end development strategy alignment at both local and global levels. · ...

The Local Safety Officer will serve as a clinical and post-marketing medical safety expert in Japan. They will be responsible for all signal management activities in the country and ensure that local product labels and risk management plans are properly aligned with the benefit r ...

Implement pharmacovigilance system for UCB products and ensure compliance with regulatory requirements. · Bachelor's Degree · HCP based education (e.g., physician, pharmacist, nurse) · ...

Develop and implement strategic plans to align brand strategy with market execution. · ...

The GCDSE provides clinical and R&D expertise in their region/country. · Accountable for global protocol development · Ensures consistency across trials in terms of site selection approval process · Responsible for country/regional interactions with regulatory authorities · ...

Reporting directly to Japan Chief Information Officer and functionally to APAC Chief Information · Security Officer this position will be responsible for all aspects of information security and technology risk management across L'Oréal Japan. · ...

+Clinical Research Specialist · 治験、市販後臨床研究および市販後調査の計画・実施・進捗管理と報告書作成 · ,担当施設における手続き業務、モニタリングならびに監査対応 · ,関連文書の作成および確認 · ,内部・外部関係者との良好な関係構築 · ,, · ...

The Deputy Country Quality Head will lead the implementation and maintenance of GxP quality systems in Japan. The role requires strong leadership skills and experience in quality system management, with a focus on compliance with health-regulated regulations. Key responsibilities ...

The Safety Specialist collaborates with teams to ensure safety communication and product stewardship. · ...

The Medical Education Specialist will drive regional medical education strategy and digital transformation across Japan. The Specialist will coordinate clinical education activities, deliver medical education events in line with strategic responsibilities. · ...

The Pricing Strategist will be responsible to achieve UCB's Pricing & Access objectives for the pipeline portfolio (with focus on BKZ, rare diseases, Briviact and Staccato in mid-term). · Central to the role will be maintaining a clear view on priority opportunities to focus on, ...

The primary purpose of a Project Manager (PM) is to ensure and elevate the level of country operations to realize patient value by transforming company's strategy into project delivery in Japan. · ...

We are seeking a Medical Writer to join our team. You will create high-quality regulatory-compliant clinical documents supporting product life cycle under supervision. · Create high-quality regulatory-compliant clinical documents supporting product life cycle under supervision. · ...

The Business Trainer Learning Solutions will work with Corporate APAC team internal external stakeholders to support learning system providing contents trainees' sustainable business growth. · ...