Yashika Sachdeva

About Yashika Sachdeva

As a Doctor of Pharmacy graduate, fascinated by how drugs affect the human body. That curiosity led me to Pharmacovigilance, where I now work as a Drug Safety Associate ensuring regulatory compliance in patient safety.With experience in Argus database, ICSR management (including triage, registration, duplicate search, book-in, data entry, MedDRA coding and data validation of ICSRs) of ICSR cases, and international drug safety regulations (including ICH guidelines on safety and efficacy, US FDA guidelines, CIOMS, and New EU PV legislation) and global team collaboration, I bring strong scientific judgment and a detail-oriented approach. Like a phoenix rising from ashes, I have transformed challenges into opportunities. With every phase, I have emerged stronger, sharpening my skills in drug safety and paving my way toward impactful roles in Medical Affairs.Let’s connect if you are working at the intersection of clinical science and medical strategy.

Experience

1. Associate, Pharmacovigilance

   Baxter International Inc.

   Feb 2025 — Present · Gurugram, IN

   Ensured high-quality safety case submissions by processing and evaluating 50+ clinical trial, spontaneous, and health authority cases using in-depth clinical research knowledge and adherence to ICH-GCP/GVP guidelines. Improved data accuracy and scientific value in pharmacovigilance reports by ensuring 100% MedDRA and WHO-DD coding compliance using clinical interpretation and quality control measures. Facilitated scientific communication by providing case insights and presenting safety findings that supported internal stakeholders and aligned with medical and regulatory messaging.

Education

• Maharishi Markandeshwar (Deemed to be University) Official

  Doctor of Pharmacy, Pharmacy

  2017 — 2023