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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。

Translational Medicine Scientist (FSP)

求人ID R0000035016 ロケーション 中国 仕事内容

KEY RESPONSIBILITIES:

  • Design, conduct and coordinate clinical and translational research activities involved in the evaluation and development of drugs within the Pfizer Oncology and non-oncology portfolio, focusing on pharmacodynamic proof-of mechanism/pharmacology, patient selection/stratification and clinical proof-of-concept (POC), and underlying disease biology of relevance to combination therapy and drug sensitivity or resistance. 
  •  Identify and evaluate candidate predictive biomarkers and develop clinical companion diagnostic tests that will appropriately transition from early to late phase clinical development. 
  • Work directly with a variety of external contract research organizations/vendors as well as academic collaborators and key opinion leaders to execute and expand clinical translational research efforts. 
  • Work collaboratively within highly integrated, multi-functional program teams that includes scientists within Discovery Research, Research Precision Medicine, Computational Biology, Clinical Pharmacology and Development Operations groups, as well as Clinicians, Statisticians, and Asset Team Leads. 

Training & Education Preferred:

  • Bachelor’s degree in one of the disciplines related to drug development or business management is required. An advanced scientific or business degree is highly desirable. 
  • Previous experience in a project management role. 

Behavioral Competencies:

  • Networking and Alliance Building: Able to work across many interfaces: clinical-regulatory; clinical-marketing; clinical-project management; clinical-development operations (biometrics, monitoring resource, study reporting) 
  • Influencing: be able to manage and motivate investigators and contract research organizations 
  • Innovation: Constantly challenge existing paradigms in clinical research and encouragebreakthrough designs; work with clinical development operations on study design, data captureand retrieval, reporting 
  • Courage with decisiveness to Act: Bias towards action to achieving goals 
  • Conflict Management: Good at focused listening; can find common ground and get cooperation with minimum noise 
  • 2 or more years’ experience in pharmaceutical industry, CRO or academia desired 

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