Regulatory Affairs Lead

2 weeks ago


London, Greater London, United Kingdom Warman O'Brien Full time

We are seeking a highly skilled Regulatory Affairs Lead to join our team at Warman O'Brien. This is an exceptional opportunity for a senior-level expert to lead our medical writing and regulatory activities, ensuring optimal resource allocation and driving business growth.

Key Responsibilities:
  • Accountable for all medical writing and regulatory tasks, providing strategic guidance to project teams on clinical trials.
  • Direct management of the Medical Writing team, fostering collaboration and innovation.
  • Maintain strong sponsor relationships, leveraging expertise to drive regulatory submissions and study documentation preparation.

Main Requirements:

  • 5-10 years of experience in authoring pharmaceutical regulatory documents across phases I-III.
  • Desired: line management experience, with a proven track record of successful team leadership.

Location: Central London (occasional on-site work required)

Estimated Salary: 95000 - 110000 per annum depending on experience.



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