Medical Writer – Clinical Medical Writing

An exciting opportunity exists for an experienced medical writer at one of the leading Clinical Research Organisations. This company has been established for over 25 years and offers a complete range of services to the pharmaceutical and biotechnology sectors. This is an excellent time to join as the company is growing and offers excellent opportunities for staff to develop their careers.

This role of Medical Writer will require you to create edit and coordinate the production of clinical documents including clinical study reports and protocols. You will be working in a team focused environment and some of your key duties will include;
•Writing clinical documents associated with submissions to regulatory authorities.
•Serving as primary the client contact
•Ensuring document content and style adheres to FDA/EMEA or other appropriate regulatory guidelines
•Providing Medical editing review of draft and final documents prepared by other writers before internal or external distribution

Suitable candidates for this medical writing opportunity should have a degree in a life science or health related science discipline. You should also have gained experience of writing clinical documents such as regulatory documents or clinical study documents.

This is an excellent opportunity to join an industry leading clinical research organisation where you will be offered excellent career progression opportunities and the chance to learn new skills. There is an excellent package on offer including a generous salary, life assurance, healthcare, pension and more.

Keywords – PVG, medical writing, medical writer, regulatory writing

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