Demo

Medical Writer

SSi People
Jersey, NJ Contractor
POSTED ON 4/4/2025
AVAILABLE BEFORE 5/3/2025
  • Candidates must be willing to work a minimum of 20 hours/week, up to 40 hours per week (hours will likely vary)

Job Responsibilities:

  • Craft comprehensive, organized, and scientifically accurate communications, ensuring consistency across all technical documentation.
  • Manage writing activities across assigned projects, ensuring alignment with business needs and adherence to medical writing strategy.
  • Served as the medical writing expert on therapeutic project teams, authoring clinical and regulatory submission documents.
  • Uphold medical writing practices/systems/tools to support clinical studies and meet company objectives.
  • Implement and maintain standardized practices across all therapeutic areas.
  • Ensure medical writing activities meet quality standards and adhere to applicable Corporate SOPs, WPs, policies, guidelines, and regulations.

Skills Required:

  • BA/BS in Life Science; graduate degree preferred.
  • 4-7 years of experience in pharmaceutical/biotechnology related to clinical research.
  • Proven expertise in writing/developing clinical documents for global regulatory submissions.
  • Ability to interpret and organize scientific and clinical data.
  • Medical writing experience in Pharma, Biotech, and/or CRO; medical device experience preferred.
  • Excellent written and verbal skills, leadership, communication, and influencing skills.


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