Senior Medical Writer

hace 2 semanas


Madrid, Madrid, España Icon A tiempo completo

About the Role

We are seeking a highly skilled Senior Medical Writer to join our team at ICON. As a key member of our clinical documentation team, you will be responsible for writing and editing high-quality clinical documents in support of regulatory submissions.

Key Responsibilities

  • Develop and implement clinical content strategies for assigned projects
  • Author and edit clinical documents, including safety summaries, efficacy summaries, and clinical overviews
  • Collaborate with cross-functional teams to ensure consistency and accuracy in clinical documentation
  • Maintain current knowledge of regulatory agency medical review guidelines and drug approval requirements

Requirements

  • 5-6 years of experience in regulatory medical writing, with 4 years of experience in writing submission documents
  • Master's degree in natural sciences or a related field; strong candidates with a Bachelor's degree will also be considered
  • Thorough understanding of the overall drug development process and clinical study report development process

Why Work at ICON?

At ICON, we offer a comprehensive and competitive total reward package that includes a wide range of variable pay and recognition programs, as well as best-in-class employee benefits and supportive policies.


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