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  • ID
    #31612272
  • Job type
    Full Time
  • Salary
    TBD
  • Source
    Agilent
  • Date
    2022-01-11
  • Deadline
    2022-03-12
 
Full Time

Vacancy expired!

As a federal contractor and healthcare company committed to protecting the health and safety of our employees, contractors, customers and communities, employees in the U.S. and Puerto Rico are required to be fully vaccinated against COVID-19, unless an approved exemption has been granted for a medical reason, sincerely held religious belief, or an employee is otherwise exempt under applicable law.

GPTW USAgilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek –– so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

We are searching for an experienced Clinical Affairs Scientist to work within the exciting field of Companion Diagnostics (CDx)! Your main responsibility will be to resolve clinical strategy in conjunction with team members to support the documentation of CDx in the field of oncology. This position requires strong support to regulatory applications and scientific marketing activities. The top candidate will have a background in clinical science/ research and working in oncology drug, biomarker, or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers, Quality Assurance representatives, and Regulatory Affairs representatives to assure compliance with internal and external requirements. If you are passionate about research and immersing yourself in studies, then we want you!

You will responsible for:

  • Scientific content of clinical project results, including scientific design and authoring of study protocols and reports
  • Developing and designing database and case report forms
  • Contributing to validation studies, cut-off determination studies, risk analysis, study quality control and surveillance analysis in clinical trials
  • Scientific validity of reported results and statistical analysis, tabulation and presentation of data
  • Writing Clinical Performance information for regulatory submissions and specific sections in Instructions for Use (IFU)
  • Preparing, revising, and maintaining standard operating procedures and guidance for the conduct of studies

Preferred candidate lives in Carpinteria or Santa Clara, CA, but remote work possible for well qualified candidates.

Vacancy expired!

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