Senior Regulatory Writer New
3 days ago
We are looking for a Senior Medical Regulatory Writer for our global health communications client that has offices based in Manchester but with fully remote working available.
Our client partners work with global pharmaceutical and biotechnology companies to provide expertise in strategic consultancy, multi-channel medical communications and regulatory documentation. Your role will be producing factual regulatory documentations in a wide range of therapy areas, making sure that all pieces of work are accurate and succinct. You will be able to use a wide range of regulatory documents, including protocols, clinical study reports, executive summaries, CTD clinical summaries, investigator brochures, clinical trial authorisations, narratives, regulatory response documents and clinical overviews. This really is a great opportunity to join an global agency that is able to grow your career further. In return you can expect, a competitive salary, ongoing training, pension, benefits, bonus and much more.
**Knowledge, Skills and Abilities**:
- Life science degree
- Previous regulatory writing experience with a medical communications agency (2 years plus)
- Excellent organisational skills
- Excellent English language and grammatical skills
- Good understanding of regulatory system
- Time management skills
- Problem-solving skills
- Communication skills
- Good attention to detail
**To be considered for this role you must live in the UK and have previous medical communications experience with an agency.**
***If are you looking to move in to an agency that is focussed and can offer career progression then please contact me for full details.
Dario Sterling-Dwen would be happy to help further on 01932 797993.
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