Medical Writer

2 months ago


California, United States Grifols Full time
About the Role

We are seeking a highly skilled Medical Writer to join our team at Grifols. As a Medical Writer, you will play a critical role in the development of clinical development documents, including final clinical study reports, abstracts, and regulatory agency submission documents.

Key Responsibilities
  • Author high-quality clinical study reports, abstracts, and regulatory documents, utilizing strong scientific and technical knowledge.
  • Collaborate with cross-functional teams to ensure timely and accurate document production.
  • Develop and maintain a deep understanding of clinical study data and medical literature.
  • Apply analytical and organizational skills to manage multiple projects and deadlines.
  • Ensure compliance with regulatory requirements and Grifols' standard operating procedures.
Requirements
  • Bachelor's degree in a science-related field, with coursework in biology, pharmacy, or a related area.
  • Advanced degree (MS, PhD, or PharmD) preferred.
  • Typically requires 5-8 years of pharmaceutical experience in clinical research and regulatory medical writing.
What We Offer

As a Medical Writer at Grifols, you will have the opportunity to work on a wide range of projects, develop your skills and expertise, and contribute to the development of innovative healthcare solutions. We offer a dynamic and supportive work environment, competitive compensation and benefits, and opportunities for professional growth and development.


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