Clinical Supplies Contractor at Penn Medicine, University of Pennsylvania Health System
Philadelphia, Pennsylvania, United States
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Summary
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Senior
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Kaitlyn Maclennan is a clinical research professional with 9 years of experience and over 4 years focused on oncology trials, specializing in Phase I–III studies, FDA audit readiness, and clinical supplies coordination. At Penn Medicine she advanced from Clinical Data Manager to Clinical Research Coordinator, managing complex lymphoma trials, regulatory start-up, and sponsor interactions to maintain ICH‑GCP compliance and audit‑ready documentation. Her NIH‑funded and public‑health work improved data accuracy by 25% and streamlined staff onboarding, reflecting a strong operational and quality assurance mindset. Recently completing a Master of Health Care Innovation at UPenn, she blends technical fluency in REDCap, SPSS, Excel, and Tableau with skills in process improvement, behavioral economics, and health policy. Now supporting clinical supplies at Novo Nordisk, she uniquely combines hands‑on trial operations with analytic rigor and a track record of presenting digital audit innovations nationally.
9 years of coding experience
5 years of employment as a software developer
Bachelor of Arts - BA, Economics, Bachelor of Arts - BA, Economics at Temple University
Master of Health Care Innovation, Master of Health Care Innovation at University of Pennsylvania
The CaSILE toolkit, a book publishing workflow employing SILE and other wizardry.
Contributions:8 commits in 7 days
pandocpublishingpdfsiletypesetting
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Kaitlyn Maclennan - Clinical Supplies Contractor at Penn Medicine, University of Pennsylvania Health System