Senior Regulatory & Medical Writing Leader

MMS is an award-winning, data-focused clinical research organization in the UK seeking a Senior Medical Writer to lead regulatory writing and mentor a team of Medical Writing professionals.

You will ensure quality and compliance across deliverables, manage client meetings and CRMs, and oversee projects from initiation to submission. Familiarity with ISO standards and FDA/GCP guidelines is preferred; strong communication and problem-solving skills are essential.

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