Cencora is actively hiring for the role of Senior Specialist, Pharmacovigilance at its Noida location under PharmaLex India Private Limited.
This is a strong opportunity for candidates with 2+ years of pharmacovigilance experience, especially those skilled in literature screening, ICSR processing, MedWatch/CIOMS reporting, and EMA MLM workflows.
If you are aiming to grow in drug safety, signal detection, and global PV operations, this role aligns perfectly with industry expectations.
🔍 Key Responsibilities – Pharmacovigilance Role
- Perform scientific literature screening using internal and external databases
- Classify and evaluate safety-relevant literature cases
- Conduct ICSR data entry into safety databases
- Prepare CIOMS I forms, MedWatch reports, and XML submissions
- Manage case processing and documentation lifecycle
- Download and review ICSRs from EMA MLM (Medical Literature Monitoring)
- Perform duplicate checks and reconciliation of safety cases
- Coordinate with clients and project management teams
- Maintain compliance with global pharmacovigilance guidelines
🎓 Qualifications Required
- Bachelor’s or Master’s degree in Life Sciences / Pharmacy
- Minimum 2 years of pharmacovigilance experience
- Understanding of:
- ICSR lifecycle
- Literature screening workflows
- EMA MLM system
- Drug safety databases
💡 Skills Required
- Strong communication & presentation skills
- Attention to detail in case processing & documentation
- Knowledge of global PV regulations (ICH, EMA, FDA)
- Ability to manage multiple safety reports and timelines
💰 Salary (Estimated)
- ₹5 LPA – ₹9 LPA (based on experience and company standards)
🌟 Why Join Cencora?
- Work with a global leader in healthcare & pharmacovigilance
- Exposure to international PV systems (EMA, global safety databases)
- Career growth in drug safety, aggregate reporting, and signal detection
- Opportunity to work in client-facing PV projects
📍 Job Location
- Noida, India (APAC Region)
📩 How to Apply
