Manager, Clinical Writing - £50k

Basic: £50k

This senior management role offers additional responsibility to an experienced clinical/medical writer who has held responsibility for preparing high level documentation for international clinical trials.

In addition to clinical writing activities you will be responsible for managing six writers based across the UK and Germany, contributing to business development activities and project managing stand alone writing projects. You will review all writing activities, assigning projects to members of the team and reviewing all documents produced. As the senior member of the team you will be responsible for preparing the high level regulatory documents including local/international marketing applications and clinical summaries for regulatory submission. This expanding company has international presence and an excellent reputation for producing high quality clinical research. The role is office based in the South West with minimal travel.

Applications are invited from clinical writers with at least four years experience in the preparation of clinical and regulatory documentation and some exposure to staff management and training. An excellent benefits package is available including relocation assistance if required.

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