Senior Medical Writer

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Barrington James
Paris
EUR 50 000 - 90 000
Faites partie des premiers candidats.
Il y a 3 jours
Description du poste

An innovative and fast-growing company at the intersection of life sciences and artificial intelligence is seeking a Senior Medical Writer to join their team in France. This position offers the unique opportunity to combine traditional medical writing expertise with cutting-edge AI-enabled solutions that are transforming the way regulatory and clinical documents are produced.

You will work closely with global pharmaceutical clients to implement an AI-powered platform that streamlines the development of regulatory submissions. This is an exciting opportunity to be part of a forward-thinking team redefining clinical content creation while delivering significant value to clients across the drug development lifecycle.

Key Responsibilities :

  • Configure and optimize AI-driven solutions to assist in the creation of regulatory documents.
  • Ensure the accuracy, consistency, and quality of documents in compliance with client and regulatory standards.
  • Review and refine documents produced by internal teams, ensuring they meet industry guidelines and client-specific requirements.
  • Collaborate with cross-functional teams, including Product Managers, Analysts, and Project Managers, to prepare and present platform demos to external stakeholders.
  • Serve as a key point of contact for external subject matter experts during collaborative sessions.
  • Mentor junior team members on best practices for writing and industry standards.
  • Stay informed about the latest trends, regulations, and documentation practices to support both internal development and client engagement.

Key Requirements :

  • Bachelor’s degree in a scientific or technical discipline (advanced degree a plus).
  • 5–7+ years of professional medical writing experience within the pharmaceutical, biotech, or CRO sector.
  • Proven experience authoring Clinical Study Reports (CSRs), Clinical Summaries, or Patient Narratives.
  • Familiarity with regulatory documentation guidelines and medical writing standards.
  • Proficient with MS Office tools and document management systems; strong general tech aptitude.
  • Excellent communication, collaboration, and presentation skills.
  • Ability to manage multiple priorities and deliver to deadlines in a fast-paced environment.
  • Passion for combining life sciences expertise with emerging technologies to deliver value to clients.
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