Dr. Neetika Khurana

Neetika Khurana, Ph.D., serves as a Scientific Consultant at Portal Innovations, LLC, where responsibilities include scientific writing, data analysis, and strategic analysis while collaborating across internal teams to support client projects and initiatives. In parallel, Neetika Khurana is a Scientific Writer at CrowdPharm, managing regulatory submissions for global markets and maintaining client relationships. Recent completion of the ORAQ Regulatory Affairs Training Program at Duke University enriched knowledge in drug and device development processes. Previous roles include Staff Scientist at Loyola University Chicago, Medical Laboratory Scientist at Rush University Medical Center, and Postdoctoral Researcher at various institutions, culminating in a robust educational background with a Ph.D. in Molecular Biology and Biotechnology from the University of Delhi.