MMS Holdings Inc, a data-focused clinical research organization with a Great Place to Work certification, invites you to join a collaborative, expert team focused on nonclinical regulatory writing.
This full-time remote UK role involves developing and managing technical nonclinical documents (eCTD modules 2.4/2.6, IBs, study reports), leading projects with regulatory timelines, and collaborating with cross-functional teams to ensure scientific integrity and compliance.
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