Remote Senior Nonclinical Writer – Lead Reg Submissions (UK)

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.

#J-18808-Ljbffr…