Regulatory Submissions Specialist — Global Clinical Research
MMS Holdings Inc
MMS Holdings Inc is seeking a Regulatory Affairs professional in the United States to join a data-focused CRO team. You will manage regulatory tracking, publish eCTD submissions, and coordinate with CROs, agents and vendors to ensure timely, compliant submissions. The role requires at least 3 years in Regulatory Affairs or related fields, strong MS Office and eCTD skills, and familiarity with FDA, GCP and ISO standards. #J-18808-Ljbffr MMS Holdings Inc
Vacancy posted 3 days ago
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