Looking for a Pharmacovigilance Analyst job in Bengaluru? Elanco Innovation And Alliance Centre has announced openings for Pharmacovigilance Analysts in Bengaluru, Karnataka. This is an excellent opportunity for professionals with experience in drug safety, adverse event case processing, Argus Safety, MedDRA coding, and ICSR management.
Candidates with backgrounds in M.Pharm, MVSc, or Veterinary Sciences and experience in pharmacovigilance operations can apply for this hybrid role. The company is looking for professionals who can manage adverse event reporting, perform seriousness and causality assessments, and support global pharmacovigilance activities.
Job Details
- Position: Pharmacovigilance Analyst
- Company: Elanco Innovation And Alliance Centre
- Location: Kadubeesanahalli, Bengaluru, Karnataka
- Job Type: Full-Time, Permanent
- Work Mode: Hybrid
- Experience Required: 1–6 Years
- Openings: 3 Positions
- Industry: Pharmaceutical & Life Sciences
- Department: Research & Development
Key Responsibilities
1. Adverse Event Case Processing
- Perform data entry of adverse event reports in the pharmacovigilance database.
- Conduct seriousness assessment and causality assessment of adverse event cases.
- Validate data against source documents and call notes.
- Assess reportability requirements and determine follow-up information needs.
- Ensure cases are complete, accurate, and submission-ready.
- Meet productivity and quality standards for pharmacovigilance case processing.
- Escalate issues that may delay regulatory submissions.
2. Global Pharmacovigilance Support
- Stay updated on global pharmacovigilance regulations and practices.
- Support internal stakeholders in GPV-related activities.
- Manage global adverse event mailboxes.
- Perform regulatory submissions of individual case safety reports (ICSRs).
- Collaborate with global pharmacovigilance teams.
3. Internal and External Collaboration
- Communicate with affiliate offices, call centers, legal teams, and customer response teams.
- Protect confidential company information.
- Ensure confidentiality agreements are in place before sharing sensitive information.
Required Skills
- Pharmacovigilance
- Drug Safety Operations
- Adverse Event Case Processing
- Individual Case Safety Reports (ICSR)
- Argus Safety Database
- MedDRA Coding
- Regulatory Reporting
- Causality Assessment
- Seriousness Assessment
- Medical Terminology
- Data Entry and Case Documentation
Educational Qualifications
Undergraduate
- BVSc (Bachelor of Veterinary Science)
Postgraduate
- M.Pharm (Any Specialization)
- MVSc (Any Specialization)
Why Join Elanco?
- Opportunity to work with a global pharmaceutical organization.
- Exposure to international pharmacovigilance regulations.
- Hybrid working environment.
- Experience in global safety databases and regulatory submissions.
- Career growth in drug safety and pharmacovigilance operations.
- Cross-functional collaboration with global teams.
Who Should Apply?
This Pharmacovigilance Analyst role is ideal for professionals who have:
- 1 to 6 years of pharmacovigilance experience.
- Experience in Argus Safety and MedDRA coding.
- Knowledge of adverse event reporting and ICSR processing.
- Understanding of medical terminology and regulatory requirements.
- Strong attention to detail and communication skills.
How to Apply
