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Principle Medical Writer
Wilmington, NC  Posted: 4/17/2019


Our Client is a  leading global contract research organization providing comprehensive, integrated drug development, laboratory and development, laboratory and lifecyle manamgent services. 
Principle Medical Writer - This is full time permanent role with our client. Work remotely.
  • Significant CSR, Protocol, and/or IB document ownership writing experience 
  • Researches, authors, and coordinates development of scientific documents, communication materials and deliverables
  • Provides substantive advice on strategy, regulations and industry best practices.
  • Manages medical writing projects by monitoring project budget parameters and delivering quality documents within agreed timelines and within client expectations.
  • Trains, directs and advises internal and external medical writing professionals.

Education and Experience:
  • Bachelor's degree in a science-related field
  • Prior experience within medical writing
  • Prior experience in managing and directing complex medical writing projects
  • Experience within a broad range of medical writing projects
  • Additional qualifications in medical writing (AMWA, RAC, etc) is advantageous
  • Broad regulatory affairs experience is an advantage
  • Advanced degree (PharmD, PhD, Masters) is preferred
  • Suitable, relevant experience working in the pharmaceutical/CRO industry is preferred

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