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.
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Senior Medical Writing & Regulatory Lead employer: MMS
At MMS, we are dedicated to creating a workplace where your expertise as a Principal Biostatistician is valued and nurtured. Our award-winning culture promotes collaboration and innovation, ensuring that you have the support and resources needed to excel in your role while contributing to meaningful projects in the clinical research field. With a strong focus on employee growth and a commitment to maintaining an inclusive environment, MMS stands out as an exceptional employer in the UK.
