Principal Regulatory Writer

As a Principal Regulatory Writer, you will play a pivotal role in translating complex scientific and clinical data into compelling regulatory documents. Your expertise will be crucial in ensuring compliance with European regulations and industry standards.

Key Responsibilities:

• Regulatory Expertise: Leverage your in-depth knowledge of European regulations to contribute to the development of high-quality regulatory documents, including but not limited to clinical study reports, regulatory submissions, protocols, investigator brochures, and marketing authorization applications.
• Technical Mastery: Dive into the technical details of scientific and clinical data, demonstrating a keen ability to synthesize and present information accurately and coherently. Stay abreast of industry advancements and regulatory updates to ensure the highest standards of technical accuracy.