Sponsor Dedicated Medical Writer II/Sr

Posted 1ds ago

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Job Description

Medical writer leading clinical, regulatory, and scientific documents for Syneos Health, a life sciences services organization. Collaborating with biopharmaceutical clients and cross-functional clinical teams.

Responsibilities:

  • Lead the clear and accurate completion of medical writing deliverables
  • Manage medical writing activities associated with individual studies
  • Coordinate medical writing activities within and across departments with minimal supervision
  • Lead resolution of client comments
  • Complete clinical, regulatory, safety, publication, and submission documents
  • Adhere to regulatory standards, ICH E3 guidelines, company SOPs, client standards, templates, authorship requirements, and style guides
  • Coordinate quality and editorial reviews
  • Manage source documentation appropriately
  • Lead team document reviews and act as a peer reviewer
  • Review statistical analysis plans and table/figure/listing specifications
  • Interact with clients and cross-functional teams in data management, biostatistics, regulatory affairs, and medical affairs
  • Perform online clinical literature searches and comply with copyright requirements
  • Identify and propose solutions to resolve issues
  • Provide technical support, training, and consultation
  • Contribute to internal materials, presentations, processes, standards, and capabilities
  • Mentor and lead less experienced medical writers on complex projects
  • Develop expertise in industry topics and regulatory requirements
  • Work within budgeted hours and communicate status and changes to medical writing leadership
  • Complete required administrative tasks and other assigned duties

Requirements:

  • 3–5 years of relevant experience in science, technical, or medical writing
  • Experience in the biopharmaceutical, medical device, or contract research organization industry required
  • Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices
  • Experience writing relevant document types
  • Extensive knowledge of English grammar
  • Ability to communicate clearly
  • Strong familiarity with AMA Manual of Style
  • Ability to work within budgeted hours and specified timeframes
  • Minimal travel may be required (less than 25%)

Benefits:

  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • Inclusive culture
  • Minimal travel may be required (less than 25%)
  • Comprehensive resources including emerging technologies, data, science and knowledge sharing
  • Career paths and employment opportunities
  • Collaborate with passionate problem solvers
  • Partner with the most diverse team of experts in the industry