Regulatory, Scientific and Medical Writer

  • Salary: On application
  • REF Number: 00050036
  • Consultant: Stephanie Maccioni
  • Contact: 01438 768713
  • Date Published: 01.04.2021
  • Sector: Genetics & Biologics
  • Location: Dublin / Remote, Ireland (Dublin area), UK Anywhere
  • Discipline: Medical Writing

CK Clinical are recruiting on an exclusive project with Boyds for a Regulatory, Scientific and Medical Writer. Boyds are a consultancy providing a wide range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices. Working with early stage biotechs, medical device companies and universities, the team supports the development of advanced therapy medicinal products (ATMPs), small molecules and biologics across a wide range of therapeutic areas.

This position can offer full home working or be based in their Dublin office.

Responsibilities:

  • Preparing a range of documents for submissions in the UK, EU and US such as clinical summaries and overviews, scientific advice briefing documents, paediatric investigation/study plans, orphan drug applications.
  • Preparing clinical documents
  • Preparing abstracts and manuscripts for
  • Project management including internal and client management
  • Scheduling and chairing roundtable meetings with

Your Background:

  • A self-starter with a proven experience in regulatory/scientific/medical writing within the biotech/pharma sector.
  • Significant experience in the preparation of key regulatory and clinical documents for complex projects.
  • Confident when interacting with clients and a willingness to take the lead in conversations

Apply: For more information or to apply for this Regulatory, Scientific and Medical Writer position, please contact StephanieMaccioni on 01438 768713 or email boyds@ckgroup.co.uk. Please quote reference 50036.

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