Medical Writer – Regulatory & Study Documentation

Meeveem Limited seeks a Medical Writer to develop and manage clinical study documents, ensuring high-quality and regulatory compliance. The ideal candidate has at least 2 years of medical writing experience in the pharmaceutical industry and possesses excellent project management and communication skills.

This role is hybrid, requiring attendance in the London office for at least 2 days per week. A Bachelor’s degree or equivalent in a scientific field is preferred to support scientific documentation goals.

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