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Centralized Monitoring Analyst (Level I & II)

  • Mid level
  • On-site
  • Full time
  • 2+ years
  • Evening shift

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About the role

Thermo Fisher Scientific supports pharmaceutical and biotechnology companies with clinical trial services. The analyst reviews trial data, characterizes potential risks, documents findings and supports monitoring review setup.

What you'll do

  • Review clinical trial data against centralized monitoring plans
  • Track issues, signals and potential risks in trial data
  • Document review results according to department procedures
  • Support risk characterization and reporting
  • Set up reviews, update department databases and pull reports

Skills

Must have

  • Clinical trial data analysis
  • Clinical trial monitoring
  • Risk characterization
  • Data documentation
  • Clinical trial protocols
  • Medical terminology

Nice to have

Tools

  • Microsoft office
  • Word
  • Excel
  • Powerpoint

Who it's for

Education
Bachelor's degree
Experience
2+ years
Languages
english
Domain
clinical trials

About Thermo Fisher Scientific

Thermo Fisher Scientific has 120 open roles in Bangalore, at Thermo Fisher Scientific India (registered office). See every Thermo Fisher Scientific role.

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