Megan

Megan is the Regulatory Specialist at Midwest Research Group, bringing expertise in ensuring clinical research studies comply with all applicable regulatory requirements and guidelines. She manages the preparation, submission, and maintenance of regulatory documents, including IRB/ethics committee submissions, amendments, and correspondence with sponsors and regulatory authorities.

Megan oversees study compliance by monitoring protocol adherence, tracking regulatory timelines, and maintaining accurate documentation. As a key liaison between the site, sponsors, and regulatory bodies, they help facilitate efficient study start-up, ongoing oversight, and smooth regulatory operations, supporting successful study execution and participant safety.