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Shaari Ginsburg-Laver

Shaari Ginsburg-Laver

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@ Clinical Trial Liaison | Patient Recruitment Specialist| Senior/Lead CRA
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Education

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UCLA

BA, Psychology -
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California State University, Northridge

Master of Arts (M.A.), Experimental Psychology -

Work Experience

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Moderna via Parexel

2024-08-01 - 2025-04-01

Moderna via Parexel

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Moderna via PPD (Contract)

2023-11-01 - 2024-05-01

Moderna via PPD (Contract)

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The Medical Affairs Company

2021-02-01 - 2023-10-01

The Medical Affairs Company

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Vertex Pharmaceuticals

2019-12-01 - 2021-02-01

Vertex Pharmaceuticals

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Ferring Pharmaceuticals

2019-04-01 - 2019-12-01

Ferring Pharmaceuticals

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Premier Research

2018-11-01 - 2019-04-01

Premier Research

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PRA Health Sciences

2015-05-01 - 2018-11-01

PRA Health Sciences

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IQVIA

2015-01-01 - 2015-05-01

IQVIA

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ICON plc

2013-07-01 - 2015-01-01

ICON plc

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Tarzana Treatment Centers

2012-07-01 - 2013-07-01

Tarzana Treatment Centers

Skills

Project Management Clinical Trial Management System (CTMS) Contract Research Organization (CRO) Communication Microsoft Office Clinical Trials Research Data Management Writing Clinical Research Healthcare Pharmaceuticals Life Sciences Oncology PowerPoint Teaching Regulatory Affairs GCP Compliance Data Collection

Summary

***Relocating the UK Spring 2025: Seeking employment on other side of the pond.*** With a solid background in clinical operations and patient recruitment strategy, my tenure as a Clinical Trial Liaison at Regeneron and as Lead CRA, Sanofi and Ferring, has honed my expertise in streamlining clinical trials. At the core of my professional ethos lies a commitment to patient safety, data integrity, and efficient regulatory operations. I team work to develop innovative strategies to enhance site selection and patient enrollment, contributing significantly to the advancement of medical research. Mastery of CTMS and EDC systems, coupled with a knack for troubleshooting recruitment challenges, has enabled me to design effective study visit guides and retention tools. Contributing to protocol development and clinical trial execution, I've supported the groundbreaking use of CRISPR/CAS-9 technology in Sickle Cell Disease trials. My dedication to the field is fueled by a passion for learning and embracing new challenges within therapeutic research. As a CRA, I'm well versed in 100% and Targeted monitoring and SDV. The principles of ICH-GCP are second nature as are all components of Microsoft Offices (i.e. Outlook, Excel, Teams). I'm familiar with most Data Capture system and Clinical Trial Management Systems (CTMS)

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