Senior Medical Writing & Regulatory Lead

MMS is a data-focused clinical research organization welcoming you to join a collaborative team in London. The role centers on regulatory and medical writing leadership for complex trial deliverables, with emphasis on quality and compliance.

We seek a senior professional with 6+ years' regulatory writing experience, strong mentoring skills, and a track record of managing client meetings and CRMs. ISO standards and CFR 21 Part 11 familiarity are highly valued.