Posted 25 days ago
Description
MMS is an award-winning, data-focused clinical research organization (CRO) with a Great Place to Work certification. This full-time, remote role for candidates based in the UK centers on developing, writing, and managing highly technical nonclinical documents.
You will lead projects, align submissions with regulatory guidelines (GLP, ICH, FDA/EMA), and author materials such as Module 2.4/2.6 eCTD documents, IBs and RTQs, collaborating across cross-functional teams and clients.
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