Senior Medical Writer - Regulatory Doc Lead (Hybrid)

A global biotechnology company is seeking a Senior Medical Writer to draft and manage clinical study documents and regulatory submissions. This hybrid role, based in Greater London, involves extensive collaboration with cross-functional teams to ensure high-quality documentation supporting drug development. The ideal candidate will have a strong background in medical writing, excellent project management skills, and the ability to clearly communicate complex information. Join us to make a meaningful impact in biopharmaceuticals.