Reference Number: JO-2308-520609
Regulatory Medical Writer
Rate: Negotiable
Job Type: Contract
Location: Central London / West End

Regulatory Writer

12 month contract

Remote working 

Offering up for £45.00 Per Hour via PAYE

We are partnered with a leading Pharmaceutical organisation who are looking for a Regulatory Writer on a 12 month contract basis working within the business’s Device Centre of Excellence. You will be responsible for writing device specific sections of combination product regulatory submissions. The preferred candidate would have a background with Regulatory Writing, having supported Module 3 eCTD submissions. 

Job Responsibilities include; 

• Prepare the device specific sections of combination product regulatory submissions

• Ensure all documents are produced according to agreed timelines

• Demonstrate proficiency with styles of writing required for regulatory documentation.

• Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external.

Candidate Requirements include; 

•  Eligibility to live and work in the United Kingdom

•  A Life Sciences degree or equivalent 

•  3-5 years Regulatory experience, preferrably in a Regulatory writing setting

•  Previous experience with combination products is preferred 

•  Ability to understand combination product and medical device technical language

If this position is of interest to yourself please forward your up to date CV to Sophie on sophie.malyon@cpl.com.

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