Vizen Life Sciences Hiring Drug Safety Associate (ICSR) | Pharmacovigilance Jobs 2026

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Hiring Drug Safety Associate (ICSR) 

Vizen Life Sciences

India

1–3 Years

Pharmacovigilance

ICSR

🏢 About Company

Vizen Life Sciences Pvt Ltd is a growing organization in the pharmacovigilance and drug safety domain, offering opportunities to work on global safety databases, ICSR processing, and regulatory compliance.

📌 Job Overview

• Role: Drug Safety Associate (ICSR)
• Qualification: B.Pharm / M.Pharm / Pharm.D
• Experience: 1–3 Years
• Job Type: Full-Time
• Domain: Pharmacovigilance / Drug Safety

🔬 Key Responsibilities

• ICSR case processing & data entry
• Adverse event triage & validation
• MedDRA coding & narrative writing
• Follow-ups and query management
• Literature search for safety cases
• Support audits and compliance activities

🎓 Eligibility Criteria

• B.Pharm / M.Pharm / Pharm.D
• 1–3 years experience in Pharmacovigilance
• Experience in safety databases preferred

💻 Required Skills

• ICSR processing workflow
• MedDRA coding knowledge
• Safety database handling
• Strong analytical skills
• Communication & documentation skills

💰 Salary & Benefits

• ₹3.2 – ₹6.5 LPA (Estimated)
• Global pharmacovigilance exposure
• Career growth in drug safety
• Regulatory and audit experience

🚀 Career Growth Insight

Drug Safety (ICSR) is one of the fastest-growing domains in pharma. You can grow into roles like:

• Senior Drug Safety Associate
• Signal Detection Specialist
• Aggregate Report Writer (PSUR, DSUR)
• PV Scientist

🎯 Interview Preparation Tips

• Revise ICSR lifecycle (valid case criteria)
• Understand MedDRA hierarchy
• Practice narrative writing
• Learn follow-up & query handling

Helpful resources:

• Pharmacovigilance Quiz
• Drug Safety Quiz
• PV Salary Guide
• Pharma Knowledge Hub

📌 Note Before You Apply:
Candidates with strong ICSR processing knowledge and hands-on experience will have higher chances of selection.

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