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| Job Location | London |
| Education | Not Mentioned |
| Salary | £60,000 - £90,000 per annum, inc benefits |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
An exciting, global biotech company is looking for experienced medical writers with the ability to understand protocol development, prepare clinical study reports, investigator brochures, responses to agencies and sections of regulatory submissions to support all phases of clinical development, responses to HTAs, EMA paediatric investigational plans, briefing documents, EU orphan drug designation documents.The successful candidate will hold a relevant PhD as well as strong medical writing experience working within biotech and orphan drugs arena.Exposure to leading medical writing project teams, broad understanding of biostatistics, regulatory requirements, medical terminology, pharmacology, drug design and study designs would be advantageous too.You must have the initiative and creativity for solving problems which affect multiple documents and a desire to to identify and drive improvements in processes across the business.Services advertised by Gold Group are those of an Agency and/or an Employment Business.We will contact you within the next 14 days if you are selected for interview. Privacy Policy.Equal Opportunity and Diversity Policy. Required skills
Keyskills :
project management leadership clinical protocol development medical writer clinical study repts clinical regulaty submissions investigat brochures responses to agencies responses to HTAs