MMS Holdings Inc is seeking a seasoned regulatory nonclinical writer to join our remote UK team. You will develop and manage highly technical nonclinical documents for INDs/CTAs/NDAs/MAAs, aligning with GLP, ICH, FDA and EMA guidelines.
You will lead projects, collaborate with cross-functional teams, and mentor others while ensuring scientific integrity and sponsor-specific formats. This full-time role offers flexibility and the opportunity to contribute to cutting-edge regulatory submissions
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