Headline

B.pharm Graduate| Certificied Pharmacovigilance Professional| ICSR Case Processing| MedDra Coding| WHO-DD| Drug and Patient Safety

About

B.Pharm graduate with hands-on training in pharmacovigilance, passionate about ensuring drug safety and patient well-being. I’ve gained practical experience in end-to-end ICSR case processing, adverse event identification, MedDRA coding, and safety narrative writing through my training at The Pharma Daily. During my time at Chandra Life Sciences, I also developed a solid foundation in GMP documentation, SOP review, and quality control processes. I bring strong analytical thinking, attention to detail, and a proactive learning mindset to everything I do. Skilled in clinical data management, medical coding, and tools like Excel, Power BI, and MedDRA, I’m eager to start my career in pharmacovigilance and contribute to regulatory compliance and patient safety.

Location

Bidar

Work experience

Pharmacovigilance Trainee at The Pharma Daily - Powered by Vigisolvo Pvt. Ltd., Jan 2026 - Mar 2026 · 3 mos, Remote, Processed and reviewed Individual Case Safety Reports (ICSRs), strengthening accuracy in adverse event documentation and supporting compliant safety reporting workflows. Contributed to case intake and data entry processes while ensuring completeness and consistency of safety data, improving case quality for downstream review. Developed practical understanding of global pharmacovigilance workflows, enabling efficient handling of safety cases aligned with regulatory expectations. Applied medical coding basics and quality checks to support precise safety data documentation, reducing potential reporting inconsistencies. Strengthened collaboration and communication skills while working within safety operations teams to ensure timely case processing. Built foundational knowledge in signal detection concepts and regulatory reporting requirements, supporting long-term drug safety monitoring.

Intern at CHANDRA LIFE SCIENCES PRIVATE LIMITED, Jun 2025 - Jul 2025 · 2 mos, Bidar, Karnataka, India, Gained hands-on exposure to pharmaceutical manufacturing workflows and GMP documentation practices, improving understanding of compliant production operations. Supported quality control activities including sampling and analytical testing, contributing to consistent quality assessment of pharmaceutical batches. Assisted in reviewing batch manufacturing records, strengthening documentation accuracy and compliance awareness. Performed sample preparation and HPLC analysis under supervision, enhancing practical analytical and quality evaluation skills. Developed understanding of how quality control processes directly impact product safety, reinforcing attention to detail and regulatory disciplin

Education

Bachelor's of Pharmacy, Rajiv Gandhi University of Health Sciences

Pre-University Course, Department of pre-university Education