Senior Regulatory Medical Writer

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We are a growing Scientific and Technology led regulatory consultancy.

To support our growth, we are currently seeking a freelance Senior Regulatory & Scientific Writer to join our expanding team. You will be responsible for producing high-quality scientific and regulatory documents that support the development and commercialization of pharmaceutical and biotechnology products across a variety of therapeutic areas.

Key Responsibilities:

• Review, develop, write, and edit various scientific and regulatory documents, including clinical study reports, investigator brochures, CTD modules, and briefing documents for EU & UK authorities.
• Ensure all documents comply with regulatory requirements, industry guidelines, and internal company standards.
• Participate in interpreting and planning data presentation for individual study reports ...