VEO Expert

1週間前


Minato 711 GlaxoSmithKline K.K. Full time

職務の目的および主な業務内容

Job Purpose & Key Responsibilities

VEO Expertは、担当品目のValue Evidence Plan (VEP)とIntegrated Evidence Plan (IEP)の内容の企画・策定

およびその計画の実行に責任を持ちます。Evidence NeedsおよびGapを評価し、製品価値を高めるための最も

適切な試験やデータベース研究の計画を組織横断チームにて企画・立案・提案し、その実行とEvidenceの公表

までの広い責任と職務をリードしていきます。

また、ワクチン領域においては、定期接種や自治体の予防接種補助金の根拠となるCost Effectivenessモデルの構築やその推定結果をEvidenceとして公表すること、ならびに臨床開発早期の段階にある製品Pipelineに

対して、日本やアジアの疫学的な視点から助言し、承認取得までの臨床開発計画におけるEvidence Gapを

評価し、製品Launchの前後に必要な最適なVEP/IEPを企画・立案・提案することが求められます。

The VEO Expert contributes to plan, develop and execute Value Evidence Plan (VEP) & Integrated Evidence Plan (IEP) in Japan for the assigned products. With thorough evaluation, the VEO Expert cross-functionally leads, coordinates, plans, implements, delivers and disseminates high quality, scientifically robust research projects (both clinical and/or database studies) and associated evidence which support demonstration of the value of GSK assets at maximum in alignment with brand strategies and company priorities.

Furthermore, in Vaccine area, the VEO Expert is expected to lead and contribute to the discussion of National Immunization Program (NIP) and vaccine subsidy by local municipality through evidence dissemination of cost effectiveness model development and associated projected estimate – as well as to contribute to early clinical development pipeline assets as an epidemiology expert in Japan/Asia and to plan, develop and propose optimal VEP/IEP before and after the product launch with thorough assessment of clinical development plan and clinical data package for obtaining new drug approval in Japan.

必要な条件 Basic Qualification

スキル Skill:

  • 臨床研究法、倫理指針等の理解 Well acquainted with Clinical Trials Act and Ethical Guideline in Japan, etc.
  • リーダーシップ Leadership
  • プロジェクトマネージメント Project management
  • コミュニケーションスキル(日本語・英語) Communication skill in Japanese and English
  • 経験 Experience:

  • 製薬業界、特にメディカルアフェアーズもしくは臨床開発の部署での業務経験 Experience in the Pharmaceutical industry, especially in Medical Affairs and Clinical Development
  • 各種試験(前向き、後ろ向き、観察研究など)のプロトコール作成経験もしくは試験実施経験 Experience in protocol development or study operation/management of various clinical studies (prospective, retrospective, observational, etc.)
  • 学位 / 資格 / 語学力 Education/Certification/Language:

  • 医学・薬学・自然科学系修士学位 Scientific master degree or equivalent experience
  • 英語(TOEIC 800点以上) English (TOEIC score, more than 800)
  • 望ましい条件 Preferred Qualification

    スキル Skill:

  • ワクチン領域で担当する疾患、ワクチンの科学や政策・規制に関する基礎知識 Know about diseases, science and policies/regulations related to Vaccine area
  • 社内および外部ステークホルダーの理解と適切なコミュニケーションとマネジメント力 Realize key internal and external experts in Vaccine area and act/manage to make a difference through appropriate communication
  • 経験 Experience:

  • データベース研究、Real-world dataの分析や実施経験 Experience in database study or Real-world data analysis and implementation/management
  • データサイエンス研究 および プロジェクト・試験の実施や推進経験 Experience in data science research and actual data science project/study implementation or management
  • 学位 / 資格 / 語学力 Education/Certification/Language:

  • 医学・薬学・自然科学系博士学位(または医師、PharmD資格) PhD in Science or equivalent. MD or PharmD preferred, but not essential
  • 高い英語力 - Versant(バーサント)スコアで70以上 または TOEFL iBTスコアで100以上 High level English skills with Versant score (more than 70) or TOEFL iBT score (more than 100)
  • Why GSK?

    Uniting science, technology and talent to get ahead of disease together.

    GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

    Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

    Important notice to Employment businesses/ Agencies

    GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.


    • VEO Expert

      2日前


      Minato 711 GlaxoSmithKline K.K. Full time

      職務の目的および主な業務内容 · Job Purpose & Key Responsibilities · VEO Expertは、担当品目のValue Evidence Planの作成および実行に責任を持ちます。Evidence needsおよびGapを評価し、製品価値を高めるための最も適切な試験計画を組織横断チームにて立案し、提案していきます。 · VEO Expert contributes to develop Japan Value Evidence Plan (J-VEP) of the assigned products. VEO Ex ...

    • VEO Expert

      1週間前


      Minato 711 GlaxoSmithKline K.K. Full time

      職務の目的および主な業務内容 · Job Purpose & Key Responsibilities · VEO Expertは、担当品目のValue Evidence Plan (VEP)とIntegrated Evidence Plan (IEP)の内容の企画・策定 · およびその計画の実行に責任を持ちます。Evidence NeedsおよびGapを評価し、製品価値を高めるための最も · 適切な試験やデータベース研究の計画を組織横断チームにて企画・立案・提案し、その実行とEvidenceの公表 · までの広い責任と職務をリードしていきます。 · ...