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パレクセルでの仕事

パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。

Site Intelligence Specialist- FSP ( Remote)

求人ID R0000036880 ロケーション 中国 仕事内容

Key Accountabilities:

Organization of data and knowledge sharing:

  • Assist Global Feasibility team in the management of data and knowledge, across due diligence activities and in special initiatives

Management of text library:

  • Help to drive efficiency and use of compelling strategy by the Strategic Feasibility team by compiling a text library of appropriately constructed, customer-focused information for incorporation into proposals, to be housed in Ombud

Management of slide library:

  • Develop a slide library to assist the strategic feasibility team in presenting compelling strategy at bid defense or other client meetings

Assist colleagues within Global Feasibility team in implementing augmented feasibility activities:

  • Support conduct of standalone or augmented feasibility services including investigator outreach surveys and Key Opinion Leader (KOL) interviews, Electronic Health Record (EHR) queries in TriNetx or other RWD sources, patient feasibility surveys in accordance with departmental guidelines and relevant Standard Operational Procedures (SOP).

Assist in scenario development:

  • Assist in development of enrolment scenarios aligned to the agreed strategy utilizing available modelling tools and techniques.

Team reporting:

  • Assist Global Feasibility Leadership with monthly reporting of KPIs to management

Management of team SharePoint, Filing systems:

  • Ensure professional SharePoint area, which is kept up to date, consolidate filing systems

Skills:

  • Autonomous, driven, competitive 
  • Independent thinker with exceptional analytical and problem-solving skills 
  • Highly organized with excellent interpersonal, presentation, oral and written communication skills
  • Strong sense of ownership and pride in quality of outputs 
  • Ability to multitask to tight timelines prioritizing workload and maintaining high quality standards 
  • A flexible attitude with respect to work assignments and new learning

Knowledge and Experience

  • Familiarity with clinical research industry and terminology
  • Fluent in written and spoken English

Education:

  • Currently undertaking or recently obtained Scientific Degree, RN or comparable life skill experience 
  • 1-2years clinical trial experience preferrable
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