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Linux Engineer

Moderna · Cambridge, MA +1 more

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OtherFull-time$109k–$175kCompany career page

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What they're looking for

  • Minimum 5 years of trial coordination experience in clinical research industry
  • Bachelor's degree in science-based subject; advanced degree preferred
  • Understanding of FDA and ICH GCP guidelines for clinical study conduct
  • Solid knowledge of drug development processes
  • Project management skills with excellent organizational abilities
  • Strong verbal and written communication skills
  • Experience in global clinical trial settings

What you'll be doing

  • Manage assigned clinical trials to ensure quality, compliance, and timely delivery of all deliverables
  • Oversee feasibility processes and coordinate with internal teams on study execution and timelines
  • Draft and maintain site materials including training documentation and support resources
  • Monitor clinical data entry, review periodic data quality, and support data review meetings
  • Ensure trial compliance with Moderna and ICH/GCP standards across multiple global regions

Privacy & handoff

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What RoleLantern checked

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