Dianne Regina V.

Provides editorial review including editing, rewriting, fact checking, annotating, and proofreading of all designated print and digital projects, with compliance to American and European pharmaceutical market regulatory guidelines. Ensures correct grammar, spelling, usage, and adherence to AMA style, brand, and agency style sheets. Verifies information as appropriate to the project. Follows project timelines and works closely with project management to assure timelines are being met.

Performed quality review of regulatory documents. Wrote and edited pre-clinical and clinical documents and safety reports ensuring adherence to FDA and ICH regulatory guidelines. Formatted safety and regulatory reports for consistency, clarity, and adherence to AMA style and various in-house and client style guides. Reviewed and summarized datasets into narrative format. Coordinated and managed various projects.