Scientist, Medical Writing

Added
less than a minute ago
Type
Full time
Salary
Salary not provided

Related skills

informed consent clinical study reports study protocols dsur investigator's brochure

πŸ“‹ Description

  • Assists in developing/reviewing clinical study docs (CSR, protocols, IC, IB, safety plans)
  • Conducts literature scans/reviews for summaries/reports
  • Incorporates team input into edits and revisions
  • Performs quality review and verification vs source data
  • Completes project/work instructions, process guidelines, SOP trainings
  • Contributes knowledge on Medical Device topics

🎯 Requirements

  • Allied health professional (MD, nurse, or pharmacist)
  • Well-versed in medical terminology and anatomy
  • Experience in copy review/copyediting
  • Strong project management skills
  • Experience in medical device or pharma sectors

🎁 Benefits

  • Daily Meal Subsidy
  • Flexible hours and work-from-home privileges
  • HMO coverage for dependents
  • Life and accident Insurance
  • 15 Sick Leave and 15 Vacation Leave
  • Monetized leave
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