Clinical Risk Evaluation Intern

Boston ScientificArden Hills, MN
22h

About The Position

Must graduate between Fall 2026 - Spring 2027 Currently pursuing a bachelor's or graduate level degree majoring in Biomedical Engineering, Bioengineering, or Life Sciences Must be able to commit to one of the following full internship program periods: May 18th - August 7th OR May 26th - August 14th Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization Must have at least 3 months or more experience reviewing clinical data, evaluations, or trials Strong analytical and quantitative skills; Excellent written and verbal communication skills; Strong computer and MS Office skills; Ability to work independently while contributing to the team goals; and Attention to detail and good organizational skills, including balancing multiple projects. Experience with reading and analysis of primary scientific literature; Familiarity with or exposure to clinical trial principles and design; Basic understanding of disease states, medical treatments, human and/or animal anatomy and physiology and how they relate to products; Experience with data analysis and extraction databases; and related work/intern experience.

Requirements

  • Must graduate between Fall 2026 - Spring 2027
  • Currently pursuing a bachelor's or graduate level degree majoring in Biomedical Engineering, Bioengineering, or Life Sciences
  • Must be able to commit to one of the following full internship program periods: May 18th - August 7th OR May 26th - August 14th
  • Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization
  • Must have at least 3 months or more experience reviewing clinical data, evaluations, or trials
  • Strong analytical and quantitative skills
  • Excellent written and verbal communication skills
  • Strong computer and MS Office skills
  • Ability to work independently while contributing to the team goals
  • Attention to detail and good organizational skills, including balancing multiple projects

Nice To Haves

  • Experience with reading and analysis of primary scientific literature
  • Familiarity with or exposure to clinical trial principles and design
  • Basic understanding of disease states, medical treatments, human and/or animal anatomy and physiology and how they relate to products
  • Experience with data analysis and extraction databases
  • related work/intern experience
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