Experience

Trilogy Writing & Consulting

• Germany
• Writing and Editing
• 1 - 100 Employee

• Senior Medical Writer II

  • Nov 2022 - Present

• Senior Medical Writer

  • Sep 2021 - Dec 2022



Certara Synchrogenix

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Senior Regulatory Writer

  • Feb 2019 - Jul 2021

  At Synchrogenix, I am a writer specializing in development and project management of large pharmacovigilance documentation, especially Periodic Benefit-Risk Evaluation Reports (PBRERs), Development Safety Update Reports (DSURs), and Risk Management Plans (RMPs; both EU and Core). I also have experience working on many other regulatory documents, including Investigator's Brochures (IBs) and Clinical Study Reports (CSRs).

• Regulatory Writer II

  • Aug 2016 - Feb 2019

• Regulatory Writer I

  • Aug 2015 - Aug 2016

• Technical Editor

  • Aug 2014 - Aug 2015

  As a technical editor, I was responsible for performing quality control (QC) checks on the full spectrum of regulatory documentation (nonclinical, clinical, and postmarketing). These QC checks included document formatting, line and copy editing, internal consistency checks, and checks to external sources.



bn

• United States
• Book and Periodical Publishing
• 100 - 200 Employee

• Retail Associate

  • Jan 2013 - Aug 2014



New Castle County (DE) Government

• United States
• Government Administration
• 500 - 600 Employee

• Marketing, Editing, and Document Design Intern

  • Feb 2014 - May 2014

  As an intern with the Community Services department, my two primary tasks were as follows: -designing documents and promotional materials in Adobe Photoshop and Adobe InDesign -copy editing the large quarterly program guide, "Happenings" As an intern with the Community Services department, my two primary tasks were as follows: -designing documents and promotional materials in Adobe Photoshop and Adobe InDesign -copy editing the large quarterly program guide, "Happenings"