MMS Holdings Inc. is a data-focused clinical research organization helping pharma, biotech and medical device clients navigate regulatory challenges from discovery to submission.
We are seeking a seasoned regulatory nonclinical writer based in the UK for a full-time, remote role. You will develop, write and manage highly technical nonclinical documents (Module 2.4/2.6, IB, nonclinical study reports) for INDs/CTAs/NDAs/BLAs/MAAs.
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