Isabella Lavia
Clinical Study Administrator, AstraZeneca
- Role
- Clinical Study Administrator at AstraZeneca
- Location
- Wilmington, DE, US
- LinkedIn followers
- 500 followers
About Isabella Lavia
I am current Senior attending West Chester University of Pennsylvania Honors College, majoring in Pharmaceutical Product Development. This program prepares me for a career in the pharmaceutical industry by providing me with a solid foundation in science, business, and regulatory affairs. I am involved in several extracurricular activities, such as Biotech & Pharmaceutical Business Club, Honors Student Association, Colleges Against Cancer, and Changing Health, Attitudes, and Actions to Recreate Girls (CHAARG), where I demonstrate my communication, teamwork, and leadership skills. My goal is to pursue a career in the pharmaceutical field, where I can apply my knowledge, skills, and passion to create innovative and impactful solutions for patients and society. I am eager to learn from experienced professionals and to explore new opportunities in this dynamic and evolving field.
Experience
Clinical Study Administrator
Aug 2025 — Present · Wilmington, DE, US
Coordinate and support daily administrative activities for four clinical trials, ensuring compliance with regulatory protocols and site requirements throughout Start Up, Maintenance, and Close Out- Maintain accurate study files and trial master documentation, adhering to Good Clinical Practice (GCP) and internal quality standards- Function as primary liaison between study sites and sponsor teams, facilitating timely dissemination of protocol updates, meeting agendas, and regulatory correspondence- Support contracting and communications with external vendors (labs, couriers, service providers) to streamline trial coordination and ensure timely sample handling- Review source documents and case report forms for completeness and accuracy prior to data entry and electronic capture; Preform quality checks (QC) utilizing eTMF/Veeva Clinical Vault
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