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Medical Evidence Delivery Lead

年収:900万 ~ 1300万

ヘッドハンター案件

部署・役職名 Medical Evidence Delivery Lead
職種
業種
勤務地
仕事内容 Japan EOR Evidence Delivery Leader(EDL) is a project leadership role in delivering sponsored scientific studies and medical evidence generation to support business and value claims, in line with strategy, governance processes and standard operation procedures.

Business Planning & Control
• EDL supports Therapeutic Area Medical Affairs(TAMA) Team in organizing the cross functional strategic evidence planning workshops for quality evidence plans
• EDL supports Business Planning Process as EOR window person for each TA team so that the Evidence Generation costs are forecasted as per the agreed evidence plans
• EDL contribute to ensure that Evidence plans/study concepts are scientifically and methodologically feasible to address research questions, feasible to time, cost, quality and capacity
• EDL works with EDOS in planning and controlling to track and manage the progress of Evidence Generation programs as per the agreed business plans (RBU2/LRP/PB)

Sponsored Study Delivery
• EDL ensures the operational/methodological feasibility of the study concepts/plans to initiate
• EDL is responsible to select the best external service providers(ESPs) as per the project requirements and manage the performance throughout the study
• EDL leads delivery of all components of a scientific study to time, quality, budget, project standards, company quality standards, and scientific requirements during the course of the study from SDC development through database lock, analysis, reporting and study closeout activities
• EDL is the cross-functional study team leader ensuring that studies are delivered by leveraging all available best practice, members’ expertise and relevant resources across the company to address research questions
• EDL contributes to uplift RWE capabilities of individuals involved in the Evidence Generation projects
労働条件 勤務地:大阪もしくは東京

勤務時間:
フレックスタイム制:始業及び終業の時刻は労働者の決定に委ねる。
フレキシブルタイム
(始業) 7時00分~10時00分
(終業) 15時00分~21時00分
コアタイム
10時00分~15時00分
休憩時間
12時30分~13時30分
所定労働時間
7時間15分

社宅:規程に基づき対象の場合は適用する。

社会保険(健康保険、厚生年金、労災保険、雇用保険) 適用する。
応募資格

【必須(MUST)】

【経験】
• > 3years Clinical Study Leader experience
o Leading protocol development, study site selection, data management, analysis, result-interpretation and reporting
• Managing CROs for clinical studies

【資格】
• Master degree in a scientific discipline

【能力】
• Clinical Study Delivery
• External Service Provider (i.e. CROs) Management
• Leadership & Communication
• Project Management

【語学】
• Practical English communication skill / TOEIC 800

【その他】
• Cross-functional Stakeholder management skill

【歓迎(WANT)】

【経験】
• Researches using statistics and epidemiology
• Working both in R&D and Medical (>3 years each)
• Line management experience
• Clinical Project Leader experience
• Working experience in global organization / teams

【資格】
• PhD in a scientific discipline or MD or MPH

【能力】
• Study Design, Statistics and Epidemiology
• Medical writing & Scientific Publication

【語学】
• Demonstrated English communication skills in Global Team or outside Japan

更新日 2020/05/01
求人番号 1355857

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