Duties: 1.Coordinate many functions of VP/ED in the dynamic environment of a new, international research and graduate training institute. Includes assisting with the preparation of plans, reports and meetings with institute staff, ministry officials, and public representatives. 2.Manage and schedule appointments, maintain calendars, coordinate correspondence, oversee travel plans. 3.Some translation and interpretation. 4.Take minutes and write reports in English and Japanese. 5.Carry out research online and in literature and prepare summaries. 6.Flexibility with working hours and some domestic and international travel Term This is a 3-year fixed term position with a 6-month probationary period with the possibility of promotion to a permanent staff, full-time position. Benefits Relocation, housing and commuting allowances, annual paid leave, summer holidays, national social insurance (shakai-hoken) includes health insurance, welfare pension insurance (kousei-nenkin-hoken), and worker’s accident compensation insurance (roudousya-saigai-hosyou-hoken). How to apply Please send resume and curriculum vitae in English and Japanese.

仕事内容　＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾ 各ビジネスファンクション（医薬品営業本部、マーケティング本部、開発、製造など）の 事業計画、分析 事業戦略への参画 会社概要　　＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾＾ 米国大手医薬品メーカーの日本法人。 グループの連絡調整機関として設立され、86年から自社販売開始。 98年、親会社が独自開発した糖尿病治療用万年筆型インスリン注入器 「ヒューマペン・エルゴ」を世界に先駆けて国内で発売。 99年肺ガン治療薬、ディスポーザプルタイプのインスリン製剤の発売を開始。

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

バイオサイエンス試薬を製造販売しております、外資系企業で、このたび画期的な体外診断薬を 初めて日本に上市いたしますので、大きなポテンシャルを持つ診断薬を導入していただける薬事申請のスペシャリストを募集しています。 ■　診断薬の許認可申請経験者 ■　製薬会社での勤務経験 ■　英語力あれば尚可

Key Responsibilities: Maintain and implement procedures and facilities that maintain the safety of all persons on and around the BST sites. Giving advice on a range of specialist areas such as fire regulations, occupational health and environmental health. Carry out regular inspections to check that policies and procedures are being properly implemented and meet statutory requirements. Keep records of findings and produce reports suggesting improvements for line management, Leadership Team and Board of Trustees. Carry out incident and accident investigations, liaising with relevant authorities. Report findings and recommendations, which are then monitored. Develop preventative and remedial programmes. Circulation of safety information Risk assessments - monitor and review both routine and one-off activities Schedule and monitor safety procedures, equipment, inspections and drills Keeping records of safety training mandating training as necessary Ensure that appropriate designated and/or qualified personnel in place to meet statutory requirements. Ensure that all personnel receive any safety codes of practice which are relevant to their work and all relevant documentation pertinent to their children is made available to parents either as hard copy or up-to-date on the website Ensure staff and parent communications chains are functional and accurate Incorporate full safety induction training for all new staff and students and run refresher sessions for current staff. Participate in Emergency Planning Meetings with the Board Subcommittee, and initiate and maintain regular cross-functional staff safety meetings ensuring that safety matters are a routine part of the whole school’s functional agenda

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

Senior Program Coordinator to work with Vice President/Executive Director of a new international science and technology research institute in Okinawa. Duties: Coordinate research and administrative programs in a dynamic new international research and graduate training institute. Includes assisting with the preparation of plans and reports with administrative and research staff, ministry officials, and public representatives. Organize and manage meetings, prepare agendas, take minutes, and write reports in English and Japanese. Carry out online and other research. Some translation and interpretation required. Flexibility with working hours and some domestic and international travel required.

【Job description】 　・market research project management starting from discussion guide drafting to report writing 　・translation of Japanese market research reports and discussion guide into English 　・Client management