If you’re a life sciences or pharmacovigilance professional ready to take the next step in your career, this opportunity could be exactly what you’ve been waiting for. A globally recognized organization, Cognizant, is hiring experienced professionals for ICSR (Individual Case Safety Report) case processing roles.
With openings in Mumbai and Hyderabad, this is a great chance to work with a reputed company while strengthening your expertise in drug safety and regulatory compliance. 🌍💊
📧 How to Apply?
If you meet the criteria and are ready for your next challenge, don’t miss out:
📩 Send your updated CV to: Omar.Ansari@cognizant.com
💡 Pro Tip: Highlight your ICSR experience, tools used (Argus, Veeva, etc.), and productivity metrics to stand out.
📌 About the Role: ICSR Case Processing
ICSR case processing is a critical function in pharmacovigilance. It involves collecting, assessing, and reporting adverse event data to ensure patient safety and compliance with global regulations.
As an ICSR professional, your work directly contributes to safer healthcare outcomes worldwide. This role is best suited for candidates with hands-on experience who can thrive in a structured, deadline-driven environment.
🎯 Key Job Highlights
✨ Position: ICSR Case Processing Associate
📍 Locations: Mumbai & Hyderabad
🏢 Work Mode: Work from Office
⏳ Experience Required: Minimum 2 Years in ICSR Processing
⚡ Joining Preference: Immediate or Early Joiners Preferred
💼 Roles & Responsibilities
As part of the pharmacovigilance team, you will:
📄 Process and review Individual Case Safety Reports (ICSRs)
🔍 Perform data entry and quality checks in safety databases
📊 Ensure compliance with global regulatory guidelines (FDA, EMA, ICH)
🧾 Code adverse events and medications using MedDRA & WHO Drug Dictionary
⏱ Meet productivity and quality benchmarks
🤝 Collaborate with cross-functional teams for case resolution
📢 Identify and escalate potential safety concerns
🧠 Skills & Qualifications Required
To succeed in this role, you should have:
🎓 Degree in Life Sciences, Pharmacy, or related field
💡 Strong understanding of pharmacovigilance processes
🖥 Experience with safety databases (Argus, ArisG, Veeva)
🧾 Knowledge of MedDRA coding and regulatory standards
✍️ Good written and verbal communication skills
🔎 Strong attention to detail and analytical ability
⏰ Ability to work under tight timelines
🌟 Why Choose Cognizant?
Joining Cognizant means more than just a job—it’s a long-term career move:
🌍 Exposure to global clinical and regulatory projects
📈 Strong career growth and internal mobility opportunities
🧑🏫 Continuous learning and upskilling programs
🤝 Inclusive and collaborative work environment
💼 Stability of a well-established multinational organization
🏙 Work Locations: Mumbai & Hyderabad
📍 Mumbai: India’s financial capital with a strong presence of pharma and CRO companies
📍 Hyderabad: Known as “Genome Valley,” a leading hub for biotech and life sciences
Working in these cities provides excellent industry exposure and networking opportunities to accelerate your career.
⚠️ Important Notes
✔ Only candidates with minimum 2 years of ICSR experience will be considered
✔ This is a work-from-office role – relocation/commuting readiness is required
✔ Early applicants may have a faster selection process 🚀
🔑 Final Thoughts
The demand for skilled pharmacovigilance professionals continues to grow, especially in ICSR case processing. This opportunity at Cognizant offers a strong platform to work in a structured, growth-oriented environment while contributing to global drug safety.
