ピックアップ求人

企業別 ピックアップ求人

インヴェンティヴ・ヘルス・ジャパン合同会社

会社概要 米国CSO業界トップシェアを誇るインヴェンティヴ・ヘルス・インクの日本法人です。
インヴェンティヴ・ヘルス・ジャパンは、研究・臨床開発(CLINICAL)から、営業・マーケティング、ブランディング(COMMERCIAL)、コンサルティング(CONSULTING)、そして市販後調査まで、医薬品の一生にわたって必要な各フェーズのサービスを“ワンストップ”で提供。インヴェンティヴ・ヘルス・ジャパンは、米国CSO(Contract Sales Organization=医薬品販売業務受託機関)業界でシェアNo.1を誇るインヴェンティヴ・ヘルス・インクの日本法人として、2009年2月に設立されました。
設立 2007年8月
資本金 5,000万円
従業員 550名

役員秘書 / Executive Assistant to GM

詳細
NEW
仕事内容 * Provide senior-level administrative and personal assistance to executive management

* Support executives in all communications (telephone, e-mails, letters, and faxes)

* Maintain executive's calendar, schedule meetings and appointments, and make travel arrangements

* Produce complex documents, correspondence, and reports utilizing word processing, presentation and spreadsheet software including tables, listings, and charts

* Edit and proof documents according to high professional standards

* Develop and maintain administrative systems to increase efficiency

* Plan meetings, prepare meeting materials and minutes and organize catering

* May plan, organize and host large corporate events and meetings
勤務地 東京

Manager, Global Safety and Pharmacovigilance(東京)

詳細
NEW
仕事内容 Job Functions
・Direct the operations of the Global Safety and Pharmacovigilance group in a region
・Provide managerial oversight of the Global Safety and Pharmacovigilance Group
・Ensure that inVentiv Health Clinical is in compliance with safety reporting requirements of regulatory authorities
・Ensure that inVentiv Health Clinical meets client expectations and requirements for safety reporting
・Provide regulatory consultation regarding safety reporting for investigational drugs
・Prepare documents describing the process for monitoring and reporting serious adverse experiences (e.g., SOPs, user manuals)
・Maintain proficiency in current knowledge of all applicable regulatory guidelines and regulations relating to safety reporting
・Act as project manager for stand-alone Safety and Pharmacovigilance projects
・Provide input to the overall processes, policies and procedures of the review and processing of safety information in the department
・Coordinate with Medical Affairs, Clinical Research and Data Management for the efficient and timely review of safety information at inVentiv Health Clinical
・Interact with clients and internal staff to provide advice and guidance on safety review issues; provide training and consultation to clients
・Assist Business Development for client development presentations that involve safety reporting as a potential service; provide adequate input into client proposals
・Remain current on global pharmacovigilance requirements and disseminate any relevant changes to affected inVentiv Health Clinical personnel
・Identify training needs in pharmacovigilance and work with Training Group to implement appropriate training
・Advise senior management on adequate budget and resource planning
・May perform database administration functions
勤務地 東京

Senior Project Manager, Global Project Management(東京、大阪)

詳細
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仕事内容 【主な業務】
プロジェクトオペレーション及びファイナンス統括業務

[Primary Function]
The position is responsible for managing and delivering the operational and financial aspects of one or more clinical studies over multiple regions and/or disciplines.

[Major Responsibilities]
-Oversee interdisciplinary clinical research programs
-Represent inVentiv Health to the customer, ensuring satisfaction levels are maintained and program deliverables are communicated effectively
-Lead clinical team to ensure quality, timelines and budget management
-Responsible for TMF Management Plan and quality and completeness of TMF for assigned projects
-Accountable for the financial performance of each project assignment
-Accountable for all project deliverables for each project assigned
-Coordinate activities and deliverables of study conduct partners and proactively identify and manage issues
-Ensure studies are conducted in compliance with GCP, relevant SOP’s and regulatory requirements.
-Accountable for maintenance of study information on a variety of database and systems
-Responsible for study management components of inspection readiness for all aspects of the study conduct
-Oversight for development and implementation of Project plans
-Plan, coordinate and present at internal and external meetings
-Direct the activities of assigned Project Support staff management
-Implement resource strategies to achieve project goals
-Developing contingency planning and risk mitigation strategies to ensure successful delivery of study goals
-Participate in bid defense meetings where presented as potential project manager/director
-Lead operational input to proposal development and pricing including proposed operations strategy
-May train and support new Project Managers
勤務地 東京

資材作成担当【東京】

詳細
NEW
仕事内容 内資系製薬企業での下記業務
・プロモーション資材、デジタルツールの作成サポート
・製品マニュアル、MR教育資材の作成サポート
・資材管理
勤務地 東京 (製薬企業プロダクトマーケティング部門での派遣就業)

教育研修担当(製薬企業への派遣就業)

詳細
NEW
仕事内容 外資系スペシャリティファーマでの下記業務
①MRへの継続的教育
②一定レベルでの教育研修等の資料作成
勤務地 東京

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