Senior Regulatory Medical Writer

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:

• The ability to Review, develop, write, and edit various scientific and regulatory documents, including clinical study reports, investigator brochures, CTD modules, briefing documents for US, 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 and summary documents for nonclinical and clinical programs.
• Assist in responding to re...