Madrigal Pharmaceuticals, Inc. seeks an Associate Director of Trial Master File Operations to lead day-to-day TMF strategy and inspection readiness. You will own TMF quality, manage FSP resources, and align processes with regulatory expectations and CDISC TMF standards. You'll partner across Clinical Operations, Quality, Regulatory, and vendors to ensure consistent TMF execution and timely issue remediation, contributing to a highly compliant trial ecosystem.

Also on the board Same function, level within a rung

Level

Lead

Location

Brooklyn, NY

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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