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Worldwide Medical Content Writer

Townsend & Associates Trenton, NJ Contractor
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Worldwide Medical Content Writer
  • Develop and update worldwide medical content (standard responses, slide decks, training modules, Q&As, etc) per clinical development program, publications, data presentations, congress activity, inquiry trends, global communication platform, product safety reports, and treatment landscape.
  • Provide literature searches, medical writing, and data accuracy review for medical content on specified assets.
  • Literature search: identify and review all relevant data through literature search to ensure clear understanding of data and articulate data required in medical content deliverables.
  • Medical writing: write concise medical standard responses in BMS format to ensure succinct, factually relevant responses available for customers.
  • Data Accuracy review: perform data accuracy review to verify all data used is correct and supported by appropriate reputable references.
  • Perform style review to verify the content meets the BMS standards.
  • Respond to escalated medical information inquiries from call center.
  • Maintenance of content trackers.
  • Support the identification of medical content for update.
  • Communicate key scientific content and publications to the organization during congresses.
  • Participate in strategic development sessions.
  • Support develop training deliverables on disease state, product overviews, and relevant market events to ensure Contact Center’s readiness to address customer inquiries.
  • Consistently maintain in-depth knowledge of relevant therapy areas, products, and objectives.
  • PharmD, PhD, or life sciences degree with a preferred minimum of 2 years’ experience in medical writing and editing in medical communications, medical education, or medical information.
  • Medical writing experience in oncology is strongly preferred Strong scientific/medical writing skills evidenced by good quality writing in medical communications and/or publications in peer-reviewed journals.
  • In-depth knowledge of Good Clinical Practices, FDA regulations, GPP3 guidelines, and the drug development process.
  • Exposure to the pharmaceutical and healthcare industry with good understanding clinical study protocols and reports, investigator brochures, publications, congress materials, etc.
  • General understanding of diseases and medical information requirements from BMS customers.
  • Familiarity with data sources (e.g. Journals, clinical study reports, product labels, regulatory and other websites).
  • Understanding of the benefits and limitations of different data sources and levels of evidence.
  • Must be able to work autonomously after receiving appropriate instruction.
  • Excellent organizational skills with ability to prioritize projects and multi-task.
  • Strong interpersonal skills required to work within cross-functional teams.

Recommended skills

Pre Clinical Development
Medical Writing
Clinical Study Reports
Drug Development
Life Sciences
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Job ID: 20-00164


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