Senior Regulatory Writer

Job Description

 

  

 

 


 

 

 

Pharma.Direct UK & Europe Ltd is bespoke Pharmaceutical recruitment consultancy based in United Kingdom/Europe. Our Client is seeking a:

 

Role:                Senior Regulatory Writer

Location:          Cheshire

  

Responsibilities:

 

·         Prepare clinical regulatory documents in a diverse range of TA’s including clinical study reports(CSR’s) and the common technical document (CTD)

·         Evaluate scientific data objectively, report results and scientific concepts in a concise and accurate manner.

·         Involved in client services and will be able to contribute to the strategic planning of regulatory submissions.

  

Requirements

 

·         Regulatory Writing experience within drug development

·         Strong scientific background

·         Degree qualified or equivalent

·         Excellent written and spoken English

·         Good working understanding of clinical development and ICH guidelines for regulatory documents

·         Project management skills and proactive

·         Travel to Europe when necessary

 

To apply

 

For further details or to apply for position please contact Fandi Hatib at Pharma Direct on fandi@pharmadirect.org.uk or call +44 1234 223359.