Project Manager

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募集要項

会社概要

同社は海外に本社を置く、グローバルな新薬の研究・開発・販売を行う先進的なバイオ医薬品企業です。

業務内容

Main responsibilities:

• Main activities
  • Supporting the growth of team members
  • Complying with and enforcing industry and company rules 
  • Budget management for assigned projects 
  • Responsibility for conducting evidence meetings in each disease area 
  • ESG budget management
  • Influence related departments, joint companies, and external stakeholders and build trust
  • Smoothly carry out assigned tasks such as research with high expertise
  • Appropriately manage the progress of reexamination applications and submit applications within 
  • the deadline.
• Evidence Solution Project Duties
  • Activities to generate evidence (data) required or needed by patients or medical professionals by conducting tests and investigations,
  • The main task is project management from the decision to conduct a study to publication.
  • In general, this is similar to the PMS work under GPSP, but Companys unique feature is that it covers not only GPSP PMS but also studies conducted by Medical Affairs.
  • Integrated management of evidence generation projects (including publications)
• Project Progress/Budget
  • All evidence generation projects involving the Medical Headquarters
  • Act as a liaison between internal and external stakeholders in evidence generation activities
  • Responsible for creating an environment in which the team can act as a think tank for internal and external regulations related to evidence generation activities, and sharing and thoroughly disseminating information (including education) to necessary internal stakeholders
  • Manage budgets as project owner
  • Facilitate cross-sectional projects within the Evidence Solutions Group
  • Facilitate cross-sectional projects within the Evidence Solutions Group for the therapeutic area in charge
  • Improve the quality of the team so that the evidence generation department of Company
  • Medical Headquarters becomes the best model representing the industry

応募条件

Minimum requirements:

• ~3 years of experience in clinical development, safety, research, etc. in the pharmaceutical industry. 
• Project management experience.
• Graduate of a science faculty
• PM experience and those with the following experience: 
  • Experience in Company Sponsored Studies and IIS conducted after marketing, or experience in protocol creation and publication for post-marketing surveillance (Experience in all study types is acceptable)
  • For those in the development department, Clinical Operation Leads interested in post-marketing evidence generation

Preferred qualifications:

• Master's or PhD preferred

給与

1000 - 1800 万円

勤務地

東京