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Principal Regulatory Writer - Full or Part Time, Greater Manchester
Client: Carrot Recruitment
Location: Greater Manchester, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Reference: 336b06c01250
Job Views: 7
Posted: 03.03.2025
Expiry Date: 17.04.2025
Job Description:
The Role
The Principal Regulatory Writer will be responsible for leading the planning and delivery of regulatory submissions and other large regulatory projects in a concise and accurate manner.
* Plan and deliver regulatory submissions on behalf of pharmaceutical clients
* Prepare clinical regulatory documents across multiple therapy areas
* Evaluate scientific data
* Work on projects independently as well as group projects
You
To apply for this role as a Principal Regulatory Writer, our client is hoping for someone with the following skills and experience:
* Regulatory writing experience
* Experience writing clinical regulatory documents to a high standard
* Strong understanding of clinical development and ICH guidelines
* Experience authoring regulatory documentation such as CTD modules, response documents, and regulatory briefing documents
* Degree educated in life sciences / pharmaceutical science
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