Rajendra Kumar Kasi

About Rajendra Kumar Kasi

With over two decades of global experience in Pharmacovigilance and drug safety, I am committed to ensuring patient well-being through robust safety strategies, innovative approaches, and regulatory excellence.My career has been dedicated to advancing drug safety worldwide—from designing and implementing risk management frameworks to building future-ready pharmacovigilance systems that harness technology and data-driven insights. I am particularly passionate about leveraging digital innovation and automation to transform PV practices, streamline compliance, and improve patient outcomes.As a leader, I focus on empowering and mentoring high-performing teams, fostering a culture of collaboration, integrity, and continuous improvement. By aligning scientific expertise with regulatory strategy, I strive to deliver patient-centric safety solutions that not only meet but exceed global compliance standards.Driven by a belief that patient safety is the foundation of healthcare progress, I continue to explore new ways to innovate, collaborate, and future-proof drug safety systems for the benefit of patients worldwide.

Experience

1. Vice President and Global Head - Pharmacovigilance

   Glenmark Pharmaceuticals

   Jul 2023 — Present · IN

   Lead global pharmacovigilance strategy and operations, ensuring end-to-end patient safety, risk management, and compliance across multiple therapeutic areas and regions. • Partner with regulatory agencies (FDA, EMA, MHRA, and others) to deliver seamless global submissions and maintain compliance with evolving guidelines. • Drive innovation and digital transformation in pharmacovigilance by integrating advanced analytics, automation, and AI into safety monitoring and reporting systems. • Build and mentor high-performing cross-functional teams, fostering a culture of collaboration, scientific rigor, and accountability. • Serve as a trusted advisor to executive leadership, aligning PV strategy with corporate objectives, market expansion, and patient-centric outcomes.

Education

• Indian Institute of Management Ahmedabad

  Certificate course, Organizational Leadership

• Jawaharlal Nehru Technological University, Hyderabad

  B. Pharmacy, Pharmaceutics, Pharmacology and Medicinal Chemistry

  1999 — 2003

• Birla Institute of Technology and Science, Pilani

  MS, Pharmaceutical operations and management

  2007 — 2009

Skills

• Glp
• Clinical Research
• Capa
• CRO
• Auditing
• Protocol
• Regulatory Affairs
• Lifesciences
• Vaccines
• Regulatory Submissions
• Standard Operating Procedure (Sop)
• Meddra
• Medical Writing
• Pharmaceutical Industry
• Sop
• Fda
• Management
• Validation
• Clinical Development
• Life Sciences
• Research
• Regulatory Requirements
• Pharmacokinetics
• Ich-Gcp
• Gcp
• Clinical Trials
• Pharmacovigilance
• Gmp