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Medical Writing Manager (Regulatory) – Global CRO – Remote (UK only) - £competitive, bonus, benefits

This is an exciting time to join this market-leading, global CRO based in the UK. You’ll be predominantly managing a team of Medical Writers but will also be involved in some writing activities/reviews.

The Company

A global, well-known CRO is now recruiting for a Medical Writing Manager (Regulatory) 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 Manager, Associate Director, and beyond
  • Great training and development

The Role

Working on a number of exciting projects and with an exciting pipeline, the Medical Writing Manager (Regulatory) will be responsible for;

  • Managing a team of Medical Writers, ranging from entry-level to Principal Writer level
  • Managing the team across multiple territories (this role will be home-based in the UK, but your team members may be based overseas)
  • Research, create and edit documents associated with the clinical sections of regulatory

submissions and other clinical documents.

  • Managing multiple projects concurrently
  • Reviewing all documentation to a high standard
  • Working across multiple therapy areas
  • Meet both internal/external deliverables against set timelines

You

To apply for this role as Medical Writing Manager (Regulatory) our client is hoping for someone with the following skills and experience

  • Ample management experience within Medical Writing
  • Ideally experience within a CRO however, Pharma and Consultancy backgrounds will also be considered
  • Experienced writing and reviewing a range of documents i.e., CSRs, Investigative Brochures, Clinical Documents, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections to Clinical Overviews
  • Broad experience in managing complex medical writing projects

What should you do next?

This Medical Writing Manager (Regulatory) role is one not to be missed; it encompasses the opportunity to work  To discuss this Medical Writing Manager (Regulatory) 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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