This is an exciting time to join an expanding, highly successful consultancy in the leafy suburbs of Greater Manchester.
They offer excellent training and development opportunities as well as great career progression opportunities.
Excellent career progression opportunities
Great training and development
Flexible working possible DoE for part of the week (not all)
Writing and editing regulatory and clinical documents, including protocols, CSRs,
submission dossiers, PIPs, etc
Creation of clinical documents in relation to regulatory projects and clinical studies
Managing and co-ordinating various regulatory writing projects
As the Medical Writer (Regulatory), you will have the following experience :
Previous regulatory / clinical writing experience (min 5 years ideally)
PhD / MD in medicine, life or health sciences, or pharmacy
Proven ability to work independently and under pressure, to strict deadlines