Enejda Subashi

Background

About Enejda Subashi

Preclinical project manager with a strong scientific background in neuroscience and gene therapy, combined with hands-on experience in drug discovery within biotechnology settings. Skilled in designing and executing in vivo studies, as well as conducting molecular, biochemical, and histological analyses to support preclinical development. Proven ability to lead complex in vivo programs and manage critical CRO partnerships, ensuring high-quality data and alignment with strategic goals. Experienced in DMTA execution from study design to data interpretation, contributing to lead optimization and candidate selection. Known for a solution-oriented mindset and a collaborative approach, I take pride in advancing therapeutic programs with scientific rigor, operational clarity, and cross-functional coordination. Core Expertise • In Vivo Pharmacology & Study Execution (rodent models, dosing, behavior, sample collection) • Molecular & Biochemical Techniques (RT-qPCR, dPCR, WB, ELISA, Jess) • Preclinical Program Management & DMTA Leadership • Biomarker Discovery & Translational Data Analysis • Scientific Communication & Regulatory Documentation