Clinical Evaluation Report Specialist

4 weeks ago


Sheffield, Sheffield, United Kingdom Publicis Groupe UK Full time
Clinical Evaluation Report Writer

We are seeking a skilled medical writer to join our team at Publicis Groupe UK. As a Clinical Evaluation Report Writer, you will be responsible for translating complex scientific and clinical information into clear and concise documents for our clients in the healthcare and pharmaceutical industries.

Key Responsibilities:
  • Prepare and edit clinical study protocols, clinical study reports, investigator brochures, and other regulatory documents for submission to health authorities.
  • Ensure that these documents comply with regulatory guidelines and standards.
  • Communicate complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.
  • Collaborate with cross-functional teams to compile and write sections of regulatory submissions, such as New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), and Investigational New Drug (IND) applications.
Requirements:
  • Native French speaker with expertise in healthcare and pharmaceutical industries.
  • Strong understanding of regulatory guidelines and standards.
  • Excellent communication and writing skills.
  • Ability to work independently and collaboratively as part of a team.
What We Offer:
  • Opportunity to work with a leading international Language Services Provider.
  • Chance to develop your skills and expertise in a dynamic and fast-paced environment.
  • Competitive salary and benefits package.


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