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Global drug and device development services

Scientific Lead-Inflammation/Immunology

Technical WritingConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • Have prior experience researching background materials and developing high-quality writing across medical publications and medical communications deliverables.
  • Have an advanced degree; a PhD is preferred, and PharmD or MD may also be considered.
  • Have prior experience in a medical publications or medical communications agency.
  • Have at least 4 years of high-level content development and management experience in a medical communications agency setting.
  • Demonstrate relevant high-level writing and review experience, including proficiency with ICMJE and GPP guidelines, reviewing and interpreting scientific and technical journal content, and knowledge of prescribed styles and formats.
  • Work efficiently with network directories and databases.
  • Be familiar with and able to use industry-standard resources such as PubMed/Medline, clinicaltrials.gov, and market intelligence or data analytics providers.
  • Work with cross-functional teams, including editorial/library services, graphics/digital services, and presentation support.
  • Have the legal right to work in the country where the role is based.

Responsibilities

  • Independently approve scientific and clinical content for assigned projects and tasks.
  • Review assigned materials for accuracy and quality, and provide scientific and therapeutic insights.
  • Review work produced by internal writers, including junior medical writers.
  • Provide product and therapy-area information and strategic insight relevant to assigned projects.
  • Fact-check assigned manuscripts.
  • Collaborate with the Scientific Manager and account managers to help ensure adherence to agreed timelines.
  • Help oversee project development from initiation to completion, including escalating issues with financial impacts.
  • Write manuscripts, posters, abstracts, slide decks, and other deliverables requiring scientific or medical writing support.
  • Identify and obtain required or helpful background materials, including materials from clients.
  • Collaborate with editorial support staff to provide necessary background and technical information.
  • Participate in onboarding and mentoring new and junior medical writers.
  • Conduct background research and provide writing support for new business proposals and organic growth opportunities.
  • Support client account team members as directed by the Scientific Manager.
  • Attend client meetings approximately once a quarter.

Desired Qualifications

  • Have 3 years of experience as a Senior Medical Writer; this is strongly preferred.
  • Hold CMPP or MAPPS certification; this is desirable.
  • Have people-management and client-relationship skills.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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