Regulatory Analyst II - 249720 - San Diego, CA

Only for registered members San Diego, CA, United States

3 weeks ago

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Job summary

This position is responsible for the regulatory lifecycle management of oncology clinical trials.

Responsibilities

  • Prepares and submits research plans protocols and regulatory documents to the IRB.
  • Drafts Informed Consent Documents (ICDs) translating complex medical procedures risks into layperson-friendly language.

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