Medical Writer

3 weeks ago


Cork, Cork, Ireland Life Science Recruitment Full time

Our client, a global pharma company based in Cork, is currently recruiting for a Medical Writer to join their team. As a medical writer, you will work with cross-functional, multidisciplinary teams to facilitate external scientific publications such as abstracts, posters, manuscripts, and presentations, as well as regulatory documents such as protocols, clinical study reports, briefing documents, regulatory responses, and marketing authorization applications. This is a contract role with hybrid working.

Responsibilities

  • Plan, write, edit, review, and coordinate the publication of scientific data through peer-reviewed journals and forums and/or regulatory documents.
  • Facilitate trial development and product registration.
  • Ensure and coordinate quality checks for accuracy, collate reviewers' comments, adjust content of documents as required based on internal/external input, and prepare the final version.
  • Ensure final documents and supporting quality check documentation (with all signatures where appropriate) are placed in the appropriate document management system.
  • Build relationships with vendors and alliance partners.
  • Maintain and enhance therapeutic area knowledge including disease state and compound for assigned projects.
  • Possess an overarching view of the compound, therapeutic area, and external environment (including competitors) with the ability to lead the scientific data disclosure planning, clinical planning, submission strategy planning, customer regulatory responses, and/or current awareness literature updates and reviews.

Requirements

  • PhD is preferred but candidates with a Bachelor's Degree or Master's Degree will be considered.
  • Graduate degree with a formal research component or in life sciences.
  • Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience (e.g., neuroscience, oncology, cardiovascular, or endocrine expertise).
  • Experience in the clinical trial process or regulatory activities.
  • Experience writing regulatory or clinical trial documents.
  • Publication experience.
  • Demonstrated mastery of written English with experience in medical, scientific, or technical writing fields (at least 1 year); professional verbal skills in English.

For further details please contact Paula O'Reilly on 087 7094141 or send CV in confidence to paula.oreilly@lifescience.ie.

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