Medical Writer - £33k

This lead role within medical writing will involve the preparation of high level regulatory and clinical documentation and mentoring less experienced writers.

As part of a multi-disciplinary project team you will take a leading role in preparing or contributing to the production of clinical documents, including clinical study reports, manuscripts for publication, protocols, investigator brochures, regulatory submissions and other clinical documentation as required. You will review clinical documents prepared by other medical writers for quality control purposes acting as mentor, giving guidance and training. This will be a client facing role and you will act as project manager on stand alone writing projects. On larger multi-service related projects you will co-ordinate resource and activities, monitoring timelines and identifying potential delays.

A minimum of two years' medical writing experience within clinical research is essential for this role, along with in depth knowledge of drug development and medical writing processes. Practical experience of writing high level clinical documentation is also required.

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