Arpita Sikka

I am a dedicated pharmacovigilance professional with over 3.7 years of experience in the pharmaceutical industry. My journey began with a Bachelor of Dental Surgery, which laid the foundation for my understanding of medical practices. I have honed my skills in various roles, most recently as a Senior Executive at Cadila Pharmaceuticals, where I performed medical reviews of ICSR, PSUR, PADER, and RMPs. My role involves training team members and responding to medical queries, ensuring compliance with current guidelines.

Prior to my current position, I worked as a Medical Reviewer at Bioclinica, where I provided medical expertise on adverse event seriousness and coding. I collaborated closely with case handlers to resolve medical queries and ensured the accuracy of case documentation. My experience also includes clinical research, where I designed and oversaw clinical trials, preparing scientific reports and safety narratives. I am passionate about leveraging my skills to make meaningful contributions to the field of pharmacovigilance.