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Italiano
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USD
Katherine K
@katherinekalait
Virtual AdministratoR, Business Content Editor, Document Formatting Specialist
Stati Uniti
Inglese
Chi sono
Hello! I’m Katherine Kalaitzidis, a regulatory affairs and document specialist with extensive experience supporting pharmaceutical and biotechnology organizations. I specialize in CMC documentation, regulatory submissions, document formatting, quality control, proofreading, data verification, and submission document management. My experience includes working with clinical, nonclinical, and CMC regulatory documents, collaborating with cross-functional teams, maintaining submission trackers, and ensuring documents meet formatting, consistency, and quality requirements.
Competenze
Katherine K
offline •
Tempo di risposta medio: 1 ora
Consulta i miei servizi
Documenti modello e formattazione
I will format edit and design microsoft word document
Documenti modello e formattazione
I will microsoft word document formatting and design
Esperienza lavorativa
QC / Medical Editor / Document Specialist
Therapeutes magazine • Full time
Oct 2020 - Present • 5 yrs 11 mos
Supported clinical, nonclinical, and CMC regulatory documentation across temporary projects for major biotechnology and pharmaceutical organizations. Key responsibilities included: Drafting cover letters and completing regulatory submission forms. Reviewing regulatory documents for content, grammar, formatting, bookmarking, and consistency. Comparing documents against source materials, including text, tables, and graphs. Identifying formatting and quality issues and providing feedback to cross-functional teams. Maintaining Excel trackers for regulatory activities. Managing documents within document-management systems. Conducting document searches and creating reports. Collaborating with teams to obtain source documents and establish submission deadlines. Supporting the development and improvement of document-management practices. Working with Documentum and Veeva/RIMS systems.
CMC Regulatory Affairs Associate II
Gilead Sciences • Full time
Dec 2014 - Present • 11 yrs 9 mos
Supported regulatory submission activities for pharmaceutical development programs and served as a point of contact for U.S. CMC regulatory activities. Key responsibilities included: Supporting regulatory submissions from preparation through completion. Serving as U.S. regional lead for selected development programs. Developing and communicating regulatory strategies. Coordinating U.S. submission preparation activities. Collaborating with authors and reviewers. Supporting IND amendments and Annual Reports. Facilitating regulatory review and approval activities.
