MMS is a data-focused clinical research organization seeking an experienced Medical Writing Lead in the UK. You will oversee regulatory writing activities, mentor colleagues, and ensure high-quality deliverables across trials and submissions.
Responsibilities include leading complex projects, coordinating with clients, and applying ISO/GCP standards to keep regulatory submissions compliant and timely. Join MMS to shape the future of clinical research.
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Senior Medical Writing & Regulatory Leader in Manchester 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.
