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Clinical Content Developer

1 week ago

Toronto, Ontario, Canada Ecrscorp Full time
Key Responsibilities of a Senior Medical Writer
  • Receive medical writing projects and project information from the Senior Director, Medical Writing and Clinical Safety Monitoring.
  • Write clinical documents such as clinical study protocols, CSRs, DSURs, integrated efficacy or safety summaries, patient narratives, manuscripts, posters, and abstracts.
  • Develop initial document shells or drafts using appropriate templates and adhering to writing styles and formats.
  • Edit assigned medical writing products to refine them before releasing for review.
Requirements and Qualifications
  • Advanced degree, Ph.D. preferred, in Clinical or Medical or Life Sciences, or Master's degree with substantial experience in the subject matter.
  • At least five years' experience in medical writing practice in the pharmaceutical clinical trial environment.
  • Experience with medical writing for clinical study reports for regulatory submission.