NEW 掲載予定期間:2022/05/18(水) ~ 2022/08/14(日)

Project Manager Project Director

※ご経験に応じてLine Managementをお任せします。 ※詳細はコンサルタントへお問い合わせください。 Oversees and manages regional clinical tri…




  • こだわり条件

    語学(英語)を生かす 年間休日120日以上 土日祝日休み

  • 仕事内容

    ※ご経験に応じてLine Managementをお任せします。

    Oversees and manages regional clinical trials under leadership direction. Responsibilities typically include contributing to the development and management of budgets timelines and quality guidelines for projects thereby ensuring that expectations are met while identifying and mitigating risks. The Associate Project Manager also compiles and drives documentation for the project ensuring the accuracy and quality of regulatory data.

    [Operational delivery]
    ・Responsible for project delivery with regards to agreed time scope cost and quality
    ・TEAM COMMUNICATION: Serve as client primary contact for areas assigned by Project Manager (PM) Senior Project Manager (SPM) or Associate Director (PD)
    ・Assist in the leadership of the core project team as directed by PM/SPM/PD to facilitate their ability to lead extended cross functional project team including the maintenance of timelines in MS Project creation of PowerPoint presentations and storyboards and maintenance and escalation of items into an ADI log and/or RACT tool
    ・Follow defined project issue escalation process and Covance's Corrective Action Issue Resolution (CAIR) process
    ・TEAM COMMUNICATION: Provide performance feedback of team members to respective supervisors
    ・COST: Interpret billing guidelines for functional area
    ・SCOPE: Under direction of PM/SPM/PD track project progress against financial milestones using applicable financial systems
    ・RISK: Under direction of PM/SPM/PD proactively lead quality control and risk assurance activities to ensure project deliverables are met according to regulatory Covance and client requirements
    ・QUALITY: Assist in the successful design implementation tracking and revision of project plans for assigned projects. Assist in ensuring that all staff allocated to assigned projects adheres to professional standards and SOPs
    ・Track and maintenance of key project performance indicators for client specified metrics

  • 職種分類

    素材・化学・食品・メディカル系技術者 > 医療・医薬・メディカル系技術者 > 研究・開発(医療・医薬・メディカル)

  • 業種分類


  • 応募条件

    ・University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing medical or laboratory technology) from an appropriately accredited institution
    ・In lieu of the above requirement candidates with five (5) or more years of relevant clinical research experience in pharmaceutical CRO industries or experience in a health care setting will be considered
    ■Minimum Required:
    ・Minimum of four (4) years of relevant clinical research experience in a pharmaceutical company/CRO.
    ・In lieu of the above requirements candidates with five (5) years supervisory experience in a health care setting and four (4) years clinical research experience (including monitoring) in the pharmaceutical or CRO industries will be considered
    ・Local project coordination and/or project management experience
    ■On the Job Experience:
    ・Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
    ・Advanced computer skills (e.g. Microsoft Word Excel Project Access and Power Point)
    ・Ability to work with minimal supervision
    ・Excellent verbal and written communication skills
    ・Ability to set clear expectations for junior staff on projects
    ・Ability to resolve project related problems and prioritizes workload for self and team
    ・Demonstrated organizational skills and the ability to prioritize multi tasks
    ・Ability to understand and work with financial information
    ・Basic knowledge of project management processes
    ・Demonstrated ability to work within a matrix system

  • 年収

    1200万円 - 1800万円

  • ポジション


  • 雇用形態


  • 勤務地

    東京都 / 大阪府

  • 勤務時間

    09:00 ~ 17:30

  • 休日・休暇


    ※有給休暇補足:初年度最大13日 /日数は入社時期により変動

  • 福利厚生

    【通勤手当】全額支給 実費精算


  • 設立


  • 資本金


  • 従業員


  • 事業概要

    医薬品開発支援サービスを世界60カ国以上に展開、社員数70 000人以上を誇るCROのリーディングカンパニー。医薬品の研究から市販化まで、開発の様々な段階に対し、統合されたサービスを提供できるCRO。※日本組織は主に3つの事業で構成されています。
    1. 前臨床 / 2. CDS(Clinical Development Service) / 3. CLS(Clinical Laboratory Services)



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  • Project Manager Project Director

    ※ご経験に応じてLine Managementをお任せします。 ※詳細はコンサルタントへお問い合わせください。 Oversees and manages regional clinical tri…

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