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    제약/바이오전문 1등 헤드헌팅사 나우팜컨설팅

    코스닥 상장사 CPM (Clinical Project Manager), 과차장급

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    등록자 : 강대필상무 23-04-26 09:28

    기본정보

    코스닥 상장사 CPM (Clinical Project Manager), 과차장급

    임상

    대리~차장

    무관

    무관

    서류전형 -> 1차면접 -> 2차면접

    영어 상

    2023-04-26

    채용시

    상세정보

    본문

    CPM (Clinical Project Manager)
    [담당업무]
    -  Manage overall clinical projects from initiation, organization of project team, conduct of clinical project,
       delivery of outcomes including CSR, timely and in compliance with applicable regulations.
    - Oversee performance of CROs, third party vendors, and field CRAs including monitoring, to ensure
      compliance with study protocol and in accordance with scope of work and in accordance with corporate timelines;
      identify areas of concern and escalate to CMO or CRO as appropriate.
    - Provides guidance, clinical trial management expertise, and direction to contract CRAs in the field and inhouse staff.
    - Assurance of regulatory compliance of investigational sites with company SOPs, EMA/FDA and ICH guidelines.
    - Review key study quality metrics (e.g., eligibility, primary endpoint data, etc.) and determine appropriate action
      in conjunction with study team (autonomy may vary with experience).
    - Investigational product(IP) accountability and reconciliation process.
    - Manage conjunction with study team(autonomy may vary with experience).
    - Responsible for review or approval of IP release packages.
    - Oversee investigator meetings.
    - Develop and administer study budgets.
    - Review and/or submission of research ethics committee/regulatory documentation.
    [지원자격]
    - Typical requires a BS or BA in a relevant scientific discipline and minimum 5 years relevant clinical experience
      in the pharmaceutical industry or academia
    - Knowledges in local regulations and ICH-GCP guidelines regarding clinical trials.
    - Excellent interpersonal skills, ability to lead multifunctional teams, and mentor junior staff.
    - Effectively solves problems and uses judgment relating to national and international regulations,
      guidelines, investigator interactions and timelines.
    - Must possess a proven ability to successfully develop, implement, manage and complete clinical trials and
      manage vendor relations.
    - Must possess a proven ability to effectively communicate scientific, medical and organizational
      concepts to internal and external customers.
    - Experience in selection and management of CROs/vendors and management of external resources.
    - Good/excellent communication skill in English.