Regulatory Affairs Specialist: Elevate Submissions
Listed on 2026-10-20
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
MMS Holdings Inc is seeking a qualified Regulatory Operations professional to join our data-focused CRO team in the United States. You will manage regulatory documents, publish submissions in eCTD format, and ensure quality control across regulatory packages for health authorities.
The role requires a college degree in science, 3+ years in regulatory affairs/publishing, and strong MS Office/Adobe Acrobat skills. ISO/GxP familiarity and coordination with CROs are preferred.
We have an opening for a Regulatory Affairs Specialist:
Elevate Submissions in Phoenix, AZ, United States within Legal, Management & Operations.
The advertised compensation is 90..
This role offers the option to work remotely.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Regulatory Affairs Specialist:
Elevate Submissions role in the description above.
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