Kranthi Kumar Jannu

WORK HISTORY

EDUCATION

ABOUT KRANTHI KUMAR JANNU

Experienced Pharmacovigilance Professional | Case Processing | Clinical Trial Safety | ICSR Submissions & Compliance With strong expertise in pharmacovigilance, I specialize in the end-to-end processing and review of Individual Case Safety Reports (ICSRs) across spontaneous, literature, and clinical trial sources. I bring a deep understanding of regulatory safety reporting and global submission workflows, ensuring accuracy, compliance, and timely delivery of critical safety data. Key Responsibilities & Strengths:Comprehensive experience in ICSR case processing Proficient in handling clinical trial safety cases and spontaneous AE reportsSolid knowledge of global regulatory requirements (FDA, EMA, MHRA, etc.)Skilled in safety database navigation and tools (Argus)Experience in electronic submissions and data exchange via E2B standardsStrong collaboration with cross-functional teams in a fast-paced environmentContinuously learning and exploring how AI and automation are transforming pharmacovigilance, with a keen interest in driving efficiency and innovation in drug safety operations.Let’s connect if you’re working in PV, drug safety, or clinical research—or exploring AI in healthcare!