Sakshi Channe

About Sakshi Channe

As a dedicated Pharmacovigilance professional at Cognizant, I specialize in ensuring drug safety through meticulous case processing and ICSR (Individual Case Safety Report) management. With a deep understanding of regulatory requirements and industry best practices, I am committed to identifying, assessing, and reporting adverse drug reactions to contribute to patient safety and compliance. My role involves processing complex safety data, managing ICSR submissions, and maintaining a high standard of accuracy and timeliness in adverse event reporting. I leverage my expertise to support both clients and internal teams in maintaining robust pharmacovigilance systems, ensuring that every case meets global regulatory standards. Passionate about enhancing drug safety and regulatory compliance, I thrive in dynamic environments and am always eager to learn and grow in the ever-evolving field of pharmacovigilance.

Experience

1. Process Executive Pharmacovigilance

   Cognizant

   Jul 2025 — Present · Pune, IN

   As a Pharmacovigilance Process Executive at Cognizant, I am responsible for ensuring the safety of pharmaceutical products by processing and evaluating adverse drug reaction (ADR) reports. My role involves case intake, data entry, quality review, and coding of safety information in compliance with regulatory standards such as FDA, EMA, and ICH guidelines. I collaborate with cross-functional teams to support safety data management and contribute to continuous quality improvement. This position enhances my knowledge of drug safety operations and strengthens my foundation in clinical and regulatory practices.

Education

• Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur

  Priyadarshini J.L.College of Pharmacy Nagpur, Bachelor of Pharmacy

• Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur

  Gurunanak college of pharmacy Nagpur , Masters in pharmacy