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Global Safety Mgr_PMS

年収:900万 ~ 1300万

ヘッドハンター案件

部署・役職名 Global Safety Mgr_PMS
職種
業種
勤務地
仕事内容 Job Summary
As part of the Japan Safety organization at our company Japan Safety PMS Project Lead is
responsible for leading assigned PMS project(s) in line with applicable corporate policies and procedures, as well as local regulations and practices, in collaboration with other functions in the local operating company, such as Safety (Pharmacovigilance), Sales & Marketing, Medical Affairs, Clinical Development, and Regulatory Affairs, external service providers (e.g., CROs), and business partner(s), when applicable, to meet business needs.
This role reports to the Japan Safety PMS Project Management Team Manager or PMS Lead.

<Key Activities>
Management and Leadership:
・Develop and maintain a budget and timeline for assigned PMS project(s).

Technical Expertise in PMS:
・Lead or contribute to process improvement initiatives or implementation of legislative
changes in PMS area.
・Provide PMS and project management expertise for PMS discussions/meetings with local regulators and in local industry organizations.
・Communicate key issues related to project management of assigned PMS activities to PMS Lead or PMS Project Management Team Manager, concerned functions and product teams (local, regional, or global), as appropriate.
・Align local PMS activities with global strategy by collaborating with applicable our
stakeholders (e.g., Global Safety Officer, Centre for Observational Research representative).

Compliance, Quality, and Regulatory:
・Contribute to the creation and maintenance of business procedure documents (e.g., SOPs, work instructions) of PMS activities.
・Plan, execute, and evaluate PMS activities for assigned project(s) by:
・Developing protocols and associated forms (e.g., questionnaires) for PMS activities in
alignment with the Japan risk management plan from scientific and clinical aspects as well as points of the regulations.
・Contributing to the development, execution, and reporting on data management plans and statistical analysis plans.
・Contributing to the selection and oversight of external service providers.
・Supporting the PMS Operations Team to ensure timely handling of contracts and payments.
・Monitoring progress of PMS activities, in collaboration with internal functions and external parties (including business partners, when applicable).
・Preparing reports for regulatory submission in accordance with applicable requirements, including those in support of re-examination dossiers.
・Building and maintaining good working relationship with external subject matter experts in collaboration with other relevant functions and business partners, when applicable.
・Collaborating to generate and provide data (e.g., publication) as a proper drug use
information with internal functions (e.g., medical affairs).
・Archiving necessary documents for PMS activities appropriately.
・Collaborating to ensure self-inspection.
・Responsible for ensuring compliance with internal business procedures and applicable local regulatory requirements (e.g., GPSP, and Good Vigilance Practice [GVP]), including
compliance related to interactions with medical institutions and healthcare professionals.
・Develop, maintain, and deliver on a training plan and its execution for personnel involved with assigned PMS activities.
・Contribute to inspection readiness efforts and other inspection/audit-related activities of assigned PMS activities.
労働条件 屋内原則禁煙
応募資格

【必須(MUST)】

・製造販売後データベース調査もしくはデータベースの臨床研究の経験をお持ちの方を歓迎します。
・Skills to manage a project (e.g. issue management, budget and timeline management)
involving multiple internal and external functions for PMS activities, which may involve
external service providers and business partners
・Ability to prepare PMS protocols and associated documents (e.g., survey questionnaires)
・Working knowledge of GPSP, GVP, and GCP (as applicable to post-marketing clinical
studies)
・English language proficiency (business discussions, reading, and writing)
・Ability to write and edit business process documents (e.g. SOPs, work instructions)
・Strong communication skills (orally and in writing)
・Working in matrix environment, communicating cross-functionally and cross-regionally
・Computers: Microsoft Outlook/ Word/ Excel/Power Point/Project
・Working knowledge of data management and statistical analysis
・Working knowledge of electronic data capture (EDC) and PMS tracking system

更新日 2020/12/02
求人番号 1582565

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