Regulatory Affairs Specialist — Drive Submissions & Compliance
Listed on 2026-10-12
-
Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
MMS is a data-focused clinical research organization seeking a Regulatory Operations professional to support submissions and health authority interactions in compliance with ICH guidelines.
You will maintain submission trackers, publish documents in eCTD format, perform QC checks, and coordinate with CROs, vendors, and local authorities to ensure timely regulatory deliverables. Strong MS Office and eCTD tooling experience is required.
We are currently recruiting a Regulatory Affairs Specialist — Drive Submissions & Compliance for our team in Chicago, IL, United States.
All applications are reviewed carefully by our team.
The position is based in Chicago, IL, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).