Medical Writer

Twitter Facebook
Wayland, MA
$1 - $1
Job Type
Direct Hire
Dec 07, 2018
Job ID
Essential Job Functions
  • Serve as the lead Clinical / Medical Report Writer contributing to a variety of documents for clinical research and regulatory purposes, including clinical research protocols, annual and final study reports, investigator’s brochures, and regulatory submissions including clinical summary reports (CSR), clinical evaluation (CER), and post-market surveillance (PMS) reports.
  • Coordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate documents.
  • Manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables.
  • Review and assist in preparation of scientific publications.
  • Prepare basic statistical analysis reports as needed.
  • Minimum of bachelor’s Degree or equivalent in scientific or medical discipline; Master's Degree preferred
  • Minimum of four years medical writing experience
  • Experience with medical devices a plusmedical
  • Excellent written communication skills
  • Experience producing high quality medical, clinical and technical documents
  • Basic project management and organizational skills 
  • Ability to prioritize and manage multiple projects 
  • Impeccable attention to detail related to consistency, grammar, syntax, and accuracy
  • Strong familiarity with Microsoft Office
  • Experience and skill performing medical literature searches (PubMed, Google Scholar, etc.) highly preferred