Lidiya Lal

Background

About Lidiya Lal

I am a dedicated healthcare professional and Clinical Pharmacist with a Master’s degree in Regulatory Affairs for Drugs, Biologics, and Medical Devices from Northeastern University. I bring a unique combination of clinical expertise, regulatory knowledge, and hands-on experience in patient care, pharmacovigilance, and drug safety. In my clinical work, I provide comprehensive support to patients across physical, psychosocial, and spiritual dimensions, fostering meaningful connections—especially for those in residential settings separated from family. I collaborate closely with interdisciplinary healthcare teams to ensure patient-centered care. As a Safety Science Analyst at Labcorp, I gained valuable exposure to regulatory documentation and submission processes, pharmacovigilance and safety reporting, and compliance with FDA, EMA, and Health Canada guidelines. I coordinated safety document shipments, prepared study files, trained PV & DSS Support Specialists, and conducted risk assessment and quality assurance activities while maintaining GCP and GMP compliance. I am skilled in data analysis, research, technical writing, and policy review, and I excel at cross-functional collaboration. My strengths include strong attention to detail, analytical and organizational skills, and excellent written and verbal communication. I am comfortable working independently or in remote environments while managing multiple tasks and projects efficiently. I am passionate about combining my clinical and regulatory expertise to improve patient outcomes, support healthcare innovation, and contribute to safer, more effective therapies.