Clinical Regulatory Expert
Mercor
$130 – $170/hour · as listed
Clinical Regulatory Expert – Remote Writing Role
Mercor is seeking an advanced-level clinical regulatory expert to support AI training and data validation work on a remote basis. In this role, you'll evaluate clinical documentation and data rooms against FDA evidentiary standards and formatting requirements, identifying compliance gaps and assessing regulatory soundness. You'll also author FDA information requests (RFIs) as part of structured AI training workflows. This position suits professionals with deep STEM expertise and extensive experience in clinical regulatory affairs who can assess documentation with precision and understand FDA submission expectations.
This is a remote, hourly position at the advanced level, offered at $130–$170/hour for approximately 40 hours per week. The work combines regulatory writing and AI data work, drawing on your domain knowledge to ensure training materials meet real-world compliance benchmarks. Ideal candidates have a background in clinical regulatory strategy, FDA submissions, or related compliance roles, and are comfortable working with structured datasets and detailed documentation review.
From the listing: Mercor marketplace · hourly · 40h/week. As a regulatory expert on this project, you would own a part in multiple workflows: 1\. Clinical Data Generation: we need to validate that each data room and its documents hold up against FDA evidentiary standards and formatting expectations, including the deliberate defects planted to test regulatory judgment. 2\. FDA RFI task authorship: you must be capable of authoring information requests an
Applications are completed on the listing’s own site. Pay is shown as posted by the source (“as listed”) or the aggregator’s estimate where marked — offers and availability change, and individual results vary.
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