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New role in Regulatory Writing - Agency - No time sheets! (Permanent)

LOCATION
Manchester, Greater Manchester, M2 2FE, United Kingdom
APPLY BY
Expired
SALARY
£35,000.00 (per Annum) - £40,000.00 (per Annum)
APPLICATIONS
0 People

My client combines strategic acumen, scientific expertise, skilled medical writing and creative flair to deliver solutions tailored to each client's specific needs. They have been on the market for almost 20 years, growing and expanding. Working with them will enhance your success for future opportunities.

How would it be to be part of an agency who is a true expert in medcomms? It will improve your skills and broaden your expertise. You will become a true expert in regulatory medcomms and work autonomously.

Requirements:

They are looking for writers looking to accelerate their career.
You have at least 2 years experience in medical regulatory writing, preparing materials to support the CT - study protocols, clinical study reports (Phases I to IV), CTD clinical summaries and overviews, investigator's brochures and updates, investigational medicinal product dossiers, clinical trial registry and database summaries, clinical trial authorization/investigational new drug applications, non-clinical reports and patient narratives.

You may have been writing for audiences including healthcare professionals and/or regularity authorities and ethics committees and are ready for a new challenge.

BENEFITS

  • 25 days annual leave plus bank holidays
  • Personal Fund, an allowance for personal progression
  • Performance-led bonuses
  • Enhanced maternity and paternity package
  • Private health care
  • Life insurance

If you are looking for a new environment working in a dynamic agency with opportunities for progression and exploration, then this is the right role for you.
Get in touch for a confidential discussion!

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