Onsite Principal Medical Writer

Posted 4 weeks ago

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About the role

  • Drive and coordinate the process to draft, review and approve written assignments.
  • Work in a matrix team to ensure delivery of high quality clinical documents.
  • Proven track record in writing clinical regulatory documents.
  • Ability to quickly assess complex situations and implement effective plans for solutions.
  • Familiarity with approaches to expedite document preparation.

Requirements

  • PhD or relevant working experience within the life sciences space.
  • Clinical regulatory writing experience in the pharmaceutical industry
  • Demonstration of leadership.
  • Experience in multicultural settings.
  • Ability to interpret, describe and document clinical data.
  • Working knowledge of International Committee for Harmonisation (ICH)/Good Clinical Practice (GCP).
  • Computer skills and general computer literacy.
  • Excellent English language skills (verbal and written).

Benefits

  • Not specified

Job title

Principal Medical Writer

Job type

Experience level

Lead

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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