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Sr. Medical Science Writer - Remote

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💎 Seniority level: Senior, 4+ years

📍 Location: United States

💸 Salary: 103200.0 - 154800.0 USD per year

🔍 Industry: Medical Device

🗣️ Languages: English

⏳ Experience: 4+ years

🪄 Skills: Data AnalysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingPresentation skillsMS OfficeResearchWritingActive listeningData visualization

Requirements:
  • Requires a Baccalaureate degree
  • Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.
  • Nice to Have: Master of Science, PhD or PharmD
  • Demonstrated scientific writing experience, expertise in literature identification and analysis, advanced presentation skills
  • Knowledge of clinical research methodology, tools, processes and regulations
  • Ability to critically analyze and interpret scientific data, understanding of statistical methods
  • Experience conducting focused literature searches on PubMed, Embase, MedLine, or other similar medical literature databases
  • Ability to build and foster relationships with KOLs and key business stakeholders.
  • Highly motivated and capable of comprehending large amounts of scientific content, which is then communicated in a clear, concise fashion
  • Neuromodulation medical device experience or other implantable medical device
Responsibilities:
  • Develop clinical strategy and author clinical documents including but not limited to clinical study synopses, clinical study reports, clinical evaluation plans/reports, annual progress reports, clinical risk benefit analyses, and clinical marketing materials.
  • Collaborate with cross-functional teams, such as marketing, sales, clinical, R&D, HE&R, Quality, Compliance and Regulatory, and may represent clinical on core teams for new product development and/or product expansions.
  • Develop and maintain strong scientific knowledge of the therapeutic area, disease state, and current competitive landscape, with the ability to effectively write key clinical deliverables/sections of regulatory submissions, including regulatory responses.
  • Develop a deep understanding of clinical data: how to interpret and effectively communicate/present the data.
  • Design literature searches using relevant key words.
  • Develop and maintain an accessible repository for relevant Medtronic and competitive literature.
  • Follow Medtronic Code of Conduct, SOPs, ICMJE and other related guidelines.
  • 25% or less domestic travel.
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