-I support regulatory dossier authoring, manage document reviews, and ensure that documents coming from Pfizer comply with internal standard and regulatory requirements. --Data verification (auditing) and document reviews
-Technical writing, editing and proofreading on regulatory documents and technical reports.
-I receive leaflets, BLA, etc. from R&D, the research and development team who conduct clinical and non-clinical trials. These documents are given to me for data verification.

-Communicate with client or other interested parties via email and telephone calls
-Conduct extensive research and interviews to ensure content is accurate
-Proofread text and edit text at various stages of the writing process and in response to feedback from writers or creative directors
-Format novel and text in stylized arrangement for publication
-Serve as a beta reader for unreleased works of literature, giving feedback from the point of view of an average reader to the author

-Head one-on-one English Immersion language and content classes based on the United States Common Core state standards
-Work Remotely to facilitate the advancement of the English Language with the student

-Accessed audio and transcript files via internal platform
-Verified and corrected the spelling of brands, products, industry terms and company names mentioned in the transcript
-Corrected the grammar and spelling in files using MS Word track changes
-Checked transcripts for readability and adherence to the AlphaSights' Style Guide
-Graded each of the reviewed files in accordance with AlphaSights' 5-point system, providing grading across key categories
-Provided feedback on the overall quality

-Coordinated an interactive learning environment that allowed students to engage in participation that helped them apply and understand concepts in science
-Successfully guided students to design experiments that tested well known scientific theories
-Taught students how to properly use, care, and handle scientific equipment
-Taught students about the role of science in economics and society as a whole

-Investigated confidential, patient prescription drug history, based on NDC codes to determine prescription fraud and drug abuse.
-Communicated with patients in relation to their prescription drug history
-Examined pharmacy claims while communicating with payors and other healthcare organizations to interpret prescription drug and medical paid claims data into meaningful, actionable information
-Navigated accounts with five specific states for medical aid. (i.e., Medicaid, Medicare, BCBS

-Edited pharmaceutical submission documents, related to the development of pharmaceutical products, that comply with FDA regulations.
-Inspected written formulas and ensured they were maintained with Framework LTC by displaying the real-time tracking dashboard
-Verified that correct medical terminology was used in SOPs and BOPs)
-Administered processes and prepare reports regarding the transfer of analytical test methods according to QA and QC to align with cGMP