Leading Bio Pharma company seeks an experienced Logistics Manager for their Japan office. Management of investigational drugs (including import and delivery) - GMP activities - Staff management in Logistics Department - Close communication with clinical supply (Forecast,Label design and others

Worlds leading Japanese pharmaceutical company is seeking an global Human Resource Manager. 1. Global HR Manager 2. Reporting to the Director of Global 3. You’d be involved in global HR issues first gaining a strong understanding of local needs and requirements for the US, EU &APAC. 4. Implement Companies HR strategy. 5. International travel required.

Our Client is a Global leader and innovator headquartered in Europe. Strong Industry reputation with leading products, people and working conditions. Sales growth has been ahead of the market average the last 5 years. Responsibilities: Manage a cross functional Project team to develop key pipeline products in Japan Plan and Manage the study group for successful results Training team (DM’s, Biostats, CRA’s, Project Leaders) when necessary High-Quality monitoring for compliance of GCP and SOP

Responsibility: - Member of the legal department in Japan. - Advise internal clients and counsel across the full range of legal and business areas. - Manage legal aspects of complex cross-border transactions in a team. - Liaise with business management and operational staff.

Serve as Senior Project Manager for international (typically intercontinental) projects for one or more clients, according to Covance Standard Operating Procedures, ICH Guidelines and GCP . Responsible for the successful conduct of assigned projects. - Serve as Senior Project Manager for assigned business development opportunities. - Liaise with senior management in the Delivery and Service Centres to ensure adequate resources are available for assigned projects. - Responsible for on time, on-budget provision of client deliverables for assigned projects - Where appropriate and as assigned, line management responsibility for the training, utilisation, development and performance review of assigned clinical research personnel

US based manufacturer and distributor of pharmaceuticals, consumer products and nutritional around the world. It is crucial for the company to continue to grow its strong business in Japan by bringing new products to market continuously and quickly. To facilitate its efforts, the company is seeking physician to play a key role in its clinical development team in Japan. - Provide detailed counsel on documentation on both Japanese and English to facilitate effective approval by the authorities. - Serve as an active participant in the management team and Japan Brand Development Committee for helping to set strategy and direction for driving the business. - Develop and communicate a compelling vision for the clinical strategy that is aligned with the overall business strategy and driven by a strong personal "teachable point of view" that motivates the team. - Build a high performance team by training and developing the staff, providing ongoing coaching and counseling, retaining the best talent through motivation and recognition, and making tough decisions on non-performers, with focus on quality and urgency. - Interface effectively with headquarters and the regional office and exert influence with authority to ensure allocation and mobilization of resources into the most appropriate areas. - Implement clinical / registration trial programs from the headquarters whose outcomes will accelerate registration of the company’s new drug entities worldwide and locally. - Develop Japanese protocols and clinical trials that are relevant to Japanese business needs and within time, budget and good clinical practice (GCP) requirements. - Build and maintain a strong relationship with Regulatory, Clinical Operation, Medical Affairs and Pharmacovigilance and other functions in the Japan organization, and with headquarter support staff, so as to capitalize on opportunities to enhance performance. - Establish and maintain excellent working relationships with opinion leaders, academic professional and government centers, organizations involved in new drug development in order to create a positive impact on the Company image and business goals. - Leverage in regulatory activities to achieve regulatory approval in a timely manner. - Facilitate publication of clinical trial results in reputable Japanese and international journals to ensure universal acceptance of data by the medical community and support for product launches and registration. - Provide support, advice and quality assurance to the sales and marketing departments.

One of the worlds leading healthcare companies specializing in aesthetic products are currently seeking an accountant to join their expanding Japanese office. Small Finance team offers the flexibility and freedom for the right candidate to expand their skills and grow with the company. Responsibility : Must possess good fundamental understanding in all facets of accounting and be proficient in any computerized bookkeeping system. Also, should have good understanding of spread sheets and preferably graphical spreadsheets. Prior experience with "QuickBooks" accounting systems a plus.

Our Client is a top US Bio Pharmaceutical firm recently established and growing quickly in Japan. They have a strong pipeline of products that address critical illnesses in young children and are seeking strong and key personnel to grow further. Department: Regulatory Affairs Responsibilities: Report direct to President and dotted line to Regulatory Head in the US. Prepare and submit registrations for Approval Applications Reporting to the authority in compliance with Japanese Laws Maintain registrations

With operations in nearly all 50 US states, our client is one of the largest providers of pharmacy and related services to long term care facilities in the US. Currently employing over 15,000 people worldwide. The Tokyo office is expanding rapidly and this role would incorporate a lot travel throughout the APAC area coordinating and monitoring clinical trials. Responsibility : Responsible for the day-to-day management of the statistical activities of the Biostatistics department. . Coordinate and/or conduct and/or participate, or manage, in any or all assigned biostatistical activities for the design, implementation, data summarization/statistical analysis and reporting of clinical trials

- Report to Head of Quality Assurance - Plan audit schedule for clinical trials. - Conduct audit (for healthcare providers, CROs, internal process 　　and documents) - Conduct training and consultation for non-QA departments. - Review SOP, WI and checklists related to QA.