Laurie Lombardo, PMP

Laurie Lombardo has a diverse work experience in the healthcare industry, with a focus on project management. Laurie currently holds the position of Director, Program Management at Invivoscribe since 2019. Laurie has been with the company since 2019, previously serving as the Associate Director / Project Management Lead and Project Manager.

Prior to joining Invivoscribe, Laurie worked at Banyan Biomarkers Inc from 2015 to 2019. Laurie started as a Project Manager and later became a Senior Project Manager. In this role, they managed projects, contract manufacturer operations, and commercialization, successfully achieving FDA clearance for the company's first in-vitro diagnostics product. Laurie also developed and managed project plans, allocated resources, and ensured adherence to company strategy and goals. Additionally, they led a cross-functional project team and implemented effective communication standards and empowerment strategies to improve team performance.

Before their time at Banyan Biomarkers, Laurie worked at Qualigen Inc. from 2011 to 2015 as a Research Scientist. In this role, they led the development and optimization activities of new products, resulting in FDA clearance for FastPack Vitamin D and hsCRP immunoassays. Laurie also coordinated cross-functional tasks and created protocols, reports, and technical briefs.

At Intertek USA dba ALTA Analytical Laboratory, Laurie held the position of Project Manager/Principal Investigator from 2008 to 2010. Laurie managed pre-clinical, clinical, and discovery studies for pharmaceutical partners' new drug development programs. Laurie also played a key role in the development and validation of immunoassays and collaborated with clients to meet their technical and analytical needs.

Earlier in their career, Laurie worked at Biosite from 2003 to 2007 as a RAIV, supervising research associates in the assay development of novel biomarker assays. Laurie also served as a liaison between R&D and HTS groups.

Lastly, Laurie worked at Hybritech / Beckman Coulter from 1991 to 2003. Laurie started as a Research Assistant and quickly earned promotions to Senior Development Scientist. Laurie led various successful projects and product launches, including Class II iTag tetramer product, PSA-MP, and free-PSA-MP diagnostics.

Overall, Laurie Lombardo's work experience highlights their expertise in project management, cross-functional team leadership, and successful product commercialization within the healthcare industry.

Laurie Lombardo, PMP holds a B.A in Animal Physiology from the University of California San Diego. In 2011-2012, they attended the Boston University Corporate Education Center, where they obtained a Certificate in Project Management. Additionally, Laurie has obtained the Project Management Professional (PMP) certification from the Project Management Institute (PMI) in November 2013.