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Job Details
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Principal Regulatory Writer - Full or Part Time



Business Type: Healthcare - Management Consultancy
Job Type: Medical Writing and Editorial
Job Level: Experienced (non manager)
Position: Full Time
Location: United Kingdom
Reference: 890073
Closing Date: 12/11/20
Job Details:

Principal Regulatory Writer - Leading Consultancy - Home Based - Full or Part Time- £neg + bens

This is an exciting time to join an expanding, highly successful Consultancy on a permanent basis based in South Manchester / Cheshire. They offer excellent training and development opportunities as well as great career progression and an excellent work/life balance. This role can be 100% remote based in the UK and can also offer part time options if required (30 hours/4 days)

  • Independently owned company
  • Excellent career progression opportunities
  • Great training and development
  • Exciting and innovative projects

The Company

This is an exciting time to join an expanding, highly successful Consultancy based in South Manchester / Cheshire. You''ll be working on exciting projects with some of the biggest, most reputable pharma clients. This role offers huge variety and great career development.

  • Highly successful Consultancy working with high profile pharmaceutical clients
  • Privately owned company
  • Highly varied role, working on exciting projects for leading pharma clients
  • Great in house support, training and development

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

What should you do next?

This Principal Regulatory Writer role is one not to be missed; it encompasses the opportunity to work in a fast paced environment on new and exciting projects. To discuss further, please submit your current CV.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there.

Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



Posted: 24/02/2021 | NPJ Ref: 266297 | NPJ Original URL
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