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Senior Medical Writer (Regulatory / Clinical) - Global CRO – Home based in UK £negotiable hourly rate

A global CRO is currently recruiting a Senior Medical Writer (Regulatory / Clinical) to join them on an initial 6 month contract. The role is 100% remote and you will need to be currently based in the UK.

The Company

A global, well known CRO are now recruiting for a Senior 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
  • Great training and development

The Role

Working on a number of exciting projects and with an exciting pipeline, the Senior 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
  • Working across multiple therapy areas
  • Meet both internal/external deliverables against set timelines

You

To apply for this role as Senior 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 Senior Medical Writer role is one not to be missed; it encompasses the opportunity to worked on exciting projects for a global CRO, covering multiple new and exciting products. To discuss this Senior Medical Writer role further or to find out about other Regulatory Writing jobs I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or 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.

Apply Now!

Job Consultant

Hayley Shayestehroo

Regulatory Affairs

Senior Consultant

hayley@carrotpharma.co.uk

01625 361072

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