MMS is a data-focused clinical research organization with a Great Place to Work certification. This full-time remote role is for candidates based in the UK and involves developing, writing and managing highly technical nonclinical documents including Module 2.4/2.6 eCTD submissions and Investigator’s Brochure content.
You will lead projects, collaborate with cross-functional teams, and ensure regulatory compliance with GLP, ICH and related guidelines, driving scientific integrity and timely
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Senior Nonclinical Regulatory Writer - Remote UK 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.
