Eli Lilly Hiring Associate – Clinical Case Management (Pharmacovigilance)
Are you seeking high-paying Eli Lilly Pharmacovigilance Jobs or Clinical Case Management Careers in Bangalore? The global pharmaceutical leader, Eli Lilly and Company, has announced recruitment for the position of Associate – Clinical Case Management based at its regional offices in Bengaluru.
This role is ideal for drug safety professionals with 3 to 8 years of experience in Individual Case Safety Report (ICSR) processing, safety database operations, medical dictionary coding, and global regulatory submissions. To prepare your profile and registration, read our comprehensive tutorial on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Associate – Clinical Case Management |
| Company | Eli Lilly and Company |
| Job Requisition ID | R-107648-1 |
| Location | Bengaluru, Karnataka, India |
| Employment Type | Full-Time |
| Experience Required | 3 to 8 Years of Pharmacovigilance Experience |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc in Life Sciences, Biotech, Micro |
| Application Deadline | June 29, 2026 |
💼 Key Responsibilities
1. ICSR Processing & Database Operations
- Process Individual Case Safety Reports (ICSRs) with high quality and accuracy, ensuring strict adherence to global regulatory timelines.
- Utilize advanced safety databases, including Argus Safety Database and Veeva Vault Safety, for case verification and data entry.
- Perform MedDRA coding using appropriate Lowest Level Terms (LLTs) and Preferred Terms (PTs) for adverse events.
- Apply WHO Drug Dictionary (WHO-DD) coding for suspect and concomitant medications.
- Draft clear, scientifically accurate, and comprehensive case narratives for clinical trials and post-marketing safety data.
2. Intake, Triage & Prioritization
- Monitor safety mailboxes and incoming sources to acknowledge and triage adverse event reports.
- Assess seriousness, expectedness, duplicate status, and causality criteria to prioritize valid ICSRs.
- Initiate follow-up activities to obtain complete clinical information for incomplete reports.
3. Regulatory Submission & QPPV Support
- Prepare expedited regulatory safety reports, including 7-day and 15-day E2B submissions and CIOMS forms.
- Transmit reports to global health authorities and track electronic submission logs and acknowledgments.
- Support activities ensuring compliance with legal EU QPPV (Qualified Person for Pharmacovigilance) safety guidelines.
Case narrative writing and dictionary coding require a deep understanding of drug safety methodologies. To prepare for drug safety interviews, check our comprehensive list of Top 100 Entry Level Pharmacovigilance Questions.
🎓 Eligibility Criteria
Candidates possessing the following qualifications are eligible to apply:
- Degrees: Bachelor's or Master's degree in Pharmacy (B.Pharm / M.Pharm), Pharm.D, B.Sc or M.Sc in Life Sciences (Biochemistry, Microbiology, Biotechnology, Biological Sciences), or equivalent healthcare degrees.
- Experience: 3 to 8 years of relevant pharmacovigilance or drug safety experience.
- Prior working knowledge of safety systems like Argus and Veeva is highly desirable.
For pharmacy professionals planning their long-term career growth, read our comparison on B.Pharm Career: India vs USA.
Required Core Skills
- Advanced understanding of ICSR triage, case processing, and regulatory compliance.
- Proficiency in MedDRA and WHO Drug Dictionary coding rules.
- Strong scientific narrative writing capabilities and medical data interpretation.
- Exceptional attention to detail and capability to work in cross-functional global teams.
💰 Salary & Compensation
- Salary Package: Competitive compensation based on experience and industry standards for mid-level drug safety roles in Bangalore.
- Comprehensive medical, dental, and vision programs.
- Retirement and pension planning benefits.
- Continuous learning, professional training, and global career pathways.
If you want to compare pharmacovigilance compensations between India and global markets, check our analysis on Pharmacovigilance Salary: India vs USA.
🌟 Why Join Eli Lilly?
- Eli Lilly is a top-tier, research-driven global biopharmaceutical innovator.
- Direct exposure to global safety databases (Argus and Veeva) and international safety protocols.
- A collaborative, values-driven workspace emphasizing patient health and inclusion.
For professionals choosing between traditional clinical settings and healthcare consulting, read our analysis on Healthcare IT vs Clinical Healthcare.
📑 Resume Tips for Eli Lilly
- Highlight your specific number of years of experience in ICSR processing, narrative writing, and coding.
- State your proficiency in safety databases like Argus or Veeva.
- Keep your CV clean, ATS-optimized, and highlight any regulatory audits or quality reviews you have supported.
🎯 Eli Lilly Case Management Interview Questions
- What are the four minimum criteria required for a valid ICSR?
- How do you assess case seriousness and expectedness in pharmacovigilance?
- Describe your experience with MedDRA coding. What is the difference between an LLT and a PT?
- Explain the E2B reporting guidelines for electronic submission of safety reports.
- How do you manage complex narratives for clinical trials involving pregnant patients or pregnancy exposures?
📌 How to Apply?
Interested and eligible drug safety professionals can apply directly through Eli Lilly's MyWorkday portal using the link below. Make sure to complete your application before the official deadline on June 29, 2026. For guidance on optimizing your application profile, read our tutorial on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. When is the application deadline?
The application portal closes on June 29, 2026.
Q. Who is eligible to apply?
Candidates with a Pharmacy or Healthcare-related degree and 3 to 8 years of experience in Pharmacovigilance operations.
Q. Where is the job location?
The role is full-time, based at Eli Lilly's offices in Bengaluru, Karnataka, India.
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