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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Senior Regulatory & Medical Writing Leader 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.
