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Job description
MMS Holdings Inc in Chicago, IL is seeking an experienced Regulatory and Medical Writing professional to lead document development for regulatory submissions. You will mentor teams, manage client expectations, and ensure adherence to quality and compliance standards.
The role requires strong writing expertise, deep knowledge of FDA regulations, and the ability to coordinate cross-functional teams from planning through submission.
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Worksite address
chicago, IL, 60290, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.