Medical Writing and Regulatory Lead

13 hours ago


London, Greater London, United Kingdom Richmond Pharmacology Full time

Richmond Pharmacology, a leading Contract Research Organisation (CRO), is seeking an experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing and regulatory teams. As a senior leader, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and compliance with regulatory standards.

The successful candidate will have at least 5 years of proven relevant experience and a relevant postgraduate qualification. A degree in a relevant scientific, medical, or life sciences subject is required. The role offers a competitive salary of £90,000-£110,000 per annum, depending on experience, plus benefits including private medical insurance, pension scheme, and 25 days' annual leave.

In this role, you will manage the entire medical writing and regulatory submissions process, liaising directly with sponsors, regulatory authorities, and ethics committees. You will be responsible for high-level Quality Control (QC) across all documents, ensuring consistency and regulatory compliance.

The key responsibilities of this role include:

  • Liaising with senior leadership to forecast and manage upcoming studies, ensuring alignment with organisational priorities and timelines.
  • Maintaining up-to-date knowledge of relevant regulatory frameworks and guidance.
  • Providing expert advice and consultation to sponsors on regulatory affairs, submissions, and medical writing strategies.
  • Ensuring overall compliance with regulatory requirements and guidance.

This is an excellent opportunity for a motivated and experienced professional to join our team and contribute to the development of life-changing therapies.



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