MMS is seeking a remote-based Senior Regulatory Nonclinical Writer in the UK to develop and manage highly technical nonclinical documents for regulatory submissions. The role requires leading projects, coordinating with cross-functional teams, and ensuring compliance with GLP, ICH, FDA, and EMA guidelines.
Applicants should have a BS in pharmacology/toxicology/biology/chemistry and 5+ years of regulatory writing experience. This is a full-time remote position suitable for UK-based candidates.
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Remote Senior Nonclinical Writer – Lead Reg Submissions (UK) 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.
