Global Regulatory Submissions Specialist

MMS Holdings Inc. is a data-driven CRO seeking a Regulatory Operations professional to manage submission lifecycle and document control. You will publish submissions in eCTD format and ensure quality and compliance across all regulatory documents. Ideal candidates have 3+ years in regulatory affairs, strong MS Office/Adobe skills, and familiarity with eCTD tools. Join a collaborative team supporting pharma, biotech, and device clients across a global footprint.