Headline

Aspiring Pharmacovigilance Associate | B.Pharm Graduate | 1000+ ICSRs Processed | MedDRA & WHO-DD Coding | VigiFlow | ADR Reporting | Signal Detection | Drug Safety & Patient Safety Enthusiast

About

I am a B.Pharm graduate with a strong interest in Pharmacovigilance and Drug Safety. Through my internship at the Indian Pharmacopoeia Commission (PvPI), I gained hands-on experience in processing 1,000+ ICSRs, MedDRA coding, VigiFlow database management, ADR reporting, signal detection, causality assessment, and narrative writing. I am also familiar with WHO-DD coding, literature screening, and regulatory pharmacovigilance workflows. My academic background, industry training, and certifications in Pharmacovigilance and Clinical Research have strengthened my understanding of patient safety and regulatory compliance. Additionally, my experience in hospital and industrial pharmacy has provided a broader perspective on medication safety and pharmaceutical operations. I am eager to begin my career as a Pharmacovigilance Associate, where I can contribute to drug safety, regulatory excellence, and improved patient outcomes while continuing to learn and grow in the field.

Location

Greater Delhi Area

Work experience

Pharmacovigilance Intern at Indian Pharmacopoeia Commission, Jun 2025 - Jul 2025 · 2 mos, Ghaziabad, • Processed and reviewed 1,000+ Individual Case Safety Reports (ICSRs) using VigiFlow, contributing to accurate adverse drug reaction (ADR) monitoring and strengthening patient safety surveillance. • Conducted case intake, validity assessment, MedDRA coding, and narrative writing to ensure high-quality safety data suitable for regulatory evaluation and signal detection activities. • Supported causality assessment and signal detection processes under the Pharmacovigilance Programme of India (PvPI), helping identify potential drug safety concerns from real-world data. • Performed WHO-DD coding and literature screening to enhance the accuracy, consistency, and completeness of pharmacovigilance case records. • Gained practical exposure to CDSCO and WHO pharmacovigilance frameworks, developing a strong understanding of global drug safety regulations, post-marketing surveillance, and regulatory compliance requirements. • Collaborated with pharmacovigilance professionals to maintain data quality and contribute to evidence-based decision-making for patient safety.

Hospital Pharmacy Trainee at Mangalam Medical & Surgical Centre - India, May 2025 - Jun 2025 · 2 mos, Rohini, • Assisted in prescription screening and medication dispensing activities, ensuring accurate drug distribution and adherence to physician instructions. • Counseled patients on medication usage, dosage schedules, and safety precautions, promoting treatment adherence and reducing the risk of medication-related errors. • Supported inventory management and stock monitoring activities to maintain uninterrupted medication availability and optimize pharmacy operations. • Maintained accurate documentation and pharmacy records in compliance with hospital protocols and regulatory requirements. • Worked closely with healthcare professionals to reinforce safe medication practices and improve the overall patient care experience. • Developed practical knowledge of hospital pharmacy workflows, drug utilization processes, and medication safety principles in a clinical setting.

Industrial Pharmacy Intern at HiGlance Laboratories Pvt Ltd, May 2024 - Jul 2024 · 3 mos, Uttar Pradesh, India, • Operated and observed analytical instruments including HPLC, UV-Visible Spectrophotometer, and FTIR, gaining hands-on experience in pharmaceutical quality control testing. • Supported GMP-compliant manufacturing activities across granulation, compression, packaging, and production operations, ensuring adherence to quality standards. • Assisted Quality Assurance teams in documentation review, SOP compliance monitoring, and process validation activities to maintain regulatory readiness. • Contributed to quality control procedures by understanding analytical testing workflows and the importance of data integrity in pharmaceutical manufacturing. • Developed a strong foundation in pharmaceutical production, quality systems, and regulatory compliance within a commercial manufacturing environment. • Enhanced understanding of the end-to-end drug manufacturing lifecycle, from raw material handling to finished product release.

Education

Bachelor of Pharmacy, Pharmacy, Sharda University, Greater Noida

Intermediate, (12th), [CBSE], The Adarsh School - India