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Job Details
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Principal Medical Writer (Regulatory / Clinical)



Business Type: Clinical Research Organisation
Job Type: Medical Writing and Editorial
Job Level: Experienced (non manager)
Position: Full Time
Salary: £negotiable + Benefits
Location: United Kingdom
Reference: 890478
Job Details:
Principal Medical Writer (Regulatory / Clinical) - Global CRO – Home based in UK, Ireland or Spain - £negotiable + private healthcare, private dental, up to 10% company contribution pension, 25 days holiday

A global CRO is currently recruiting a Principal Medical Writer (Regulatory / Clinical) to join them on a permanent basis. The role is 100% remote and you will need to be currently based in the UK, Ireland or Spain.

The Company

A global, well known CRO are now recruiting for a Principal Medical Writer (Regulatory / Clinical) to join their already well-established team. Offering great training and development, this company has a huge interest in developing their employees to a high standard.
·  Global CRO
·  Working across multiple therapy areas
·  Very exciting projects to work on and upcoming pipeline
·  Excellent career progression opportunities to Senior Regulatory Writer and beyond
·  Great training and development

The Role

Working on a number of exciting projects and with an exciting pipeline, the Principal Medical Writer (Regulatory / Clinical) will be responsible for;
·  Writing, editing, and reviewing documents such as Clinical Study Report, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical Overviews etc and more
·  Managing multiple projects concurrently
·  Reviewing all documentation to a high standard
·  Working across multiple therapy areas
·  Meet both internal/external deliverables against set timelines
·  Working closely with others in the writing team e.g. Senior Regulatory Writer


You

To apply for this role as Principal Medical Writer (Regulatory / Clinical) our client is hoping for someone with the following skills and experience;

·  Ample experience in a Medical Writing / Regulatory Writing role
·  Experienced within a CRO or Pharma setting
·  Experienced writing, editing, and reviewing documents such as Clinical Study Report, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical Overviews
·   Can work in a fast-paced environment, meeting internal and external deliverables
·   Can manage multiple projects at once
·   Any therapy area experience will be considered within CRO or Pharma

What should you do next?

This Principal Medical Writer (Regulatory / Clinical) role is one not to be missed; it encompasses the opportunity to work in a global CRO, across multiple therapy areas and with a range of clients.  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: 08/07/2021 | NPJ Ref: 275114 | NPJ Original URL
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