Pharmacovigilance Literature Surveillance & Reconciliation Analyst

Roles & Responsibilities
• Support the business process owner for literature surveillance activities
• Manage training documentation and user access for literature surveillance and reconciliation systems
• Perform operational activities including literature reconciliation, quality control of non-ICSR literature, and article uploads
• Conduct ICSR reconciliation, quality monitoring, and safety spot checks in collaboration with cross-functional teams
• Handle team mailboxes and ensure timely action on all pharmacovigilance communications
• Ensure end-to-end compliance with global pharmacovigilance regulations across the literature surveillance lifecycle

Qualification
• B.Pharm / M.Pharm / Pharm.D / MSc / BSc / Life Sciences / Medicine

Experience
• Minimum 3 years of experience in a pharmacovigilance environment
• Proven experience in literature safety surveillance and ICSR reconciliation
• Exposure to global drug safety regulations for clinical and post-marketing products

Skills
• Strong knowledge of global pharmacovigilance regulations and safety reporting requirements
• Hands-on experience with literature surveillance and reconciliation processes
• Experience with ArisG Safety Database (preferred)
• Excellent written and verbal communication skills
• Ability to work effectively in a global, cross-functional matrix environment

About the Company
Merck is a global science and technology leader operating across healthcare, life science, and electronics, committed to innovation, patient safety, and advancing human health through cutting-edge research and global collaboration.