Teams at Trilogy Innovations

Edits and proofreads promotional materials for global pharmaceutical clients, ensuring grammatical accuracy, consistency, regulatory compliance, and adherence to AMA, brand, and client style guides. Formats documents for journal and congress guidelines, implements MLR review comments, and verifies approved content. The role also involves client communication, team collaboration, mentoring, knowledge sharing, training support, and contributing to continuous improvement initiatives.

Leads and builds a global CMC regulatory writing team, overseeing quality, timelines, processes, and operational standards. Provides client-facing CMC consulting, regulatory strategy input, project scoping, proposals, and presentations. Reviews and prepares complex CMC documentation while advising AI development teams on CMC-generated content. Collaborates with regulatory, manufacturing, QA/QC, CRO, operations, and commercial teams to expand CMC capabilities and service offerings.