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Senior Medial Writer



Business Type: Clinical Research Organisation
Job Type: Regulatory Affairs
Job Level: Experienced (non manager)
Position: Full Time
Salary: £Negotiable DoE
Location: United Kingdom
Reference: 889385
Closing Date: 09/12/19
Job Details:

Senior Medial Writer - Regulatory/Clinical - Global CRO - Homebased - £negotiable

Senior Medial Writer - Regulatory/Clinical, responsible for researching, creating and editing all documents associated with clinical research.

The Company

My client is a CRO covering multiple therapy areas. Based in the South East, this company have an exciting and broad variety of projects to work on.

  • Global, leading CRO
  • Home based position
  • Great career progression

The Role

The Senior Medial Writer - Regulatory/Clinical will be responsible for researching, creating and editing all documents associated with clinical research.

  • Writing Clinical Study Reports, Protocols, Informed Consent to Clinical Overviews etc
  • Managing multiple projects
  • Reviewing all documentation to a high standard

You

To apply for this role as a Senior Medial Writer - Regulatory/Clinical, our client is hoping for someone with the following skills and experience;

  • 2 years'' experience within a CRO Medical writing position
  • Good stakeholder management
  • Can work independently
  • Degree educated in life sciences

What should you do next?

This Senior Medial Writer - Regulatory/Clinical role is one not to be missed; it encompasses the opportunity to work with new and exciting products within a company who are at the forefront of clinical research. 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: 11/11/2019 | NPJ Ref: 244933 | NPJ Original URL
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