MMS is seeking a regulatory nonclinical writer for a full-time remote role based in the UK. You will develop and manage highly technical nonclinical documents for regulatory submissions, ensuring scientific integrity and compliance with GLP, ICH, FDA and EMA guidelines.
Ideal candidates have 5+ years in regulatory nonclinical writing, strong MS Office skills, and proven ability to lead complex projects across cross-functional teams within a CRO environment.
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Senior Nonclinical Writer — Lead Submissions (Remote) in Swansea 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.
