Elanco Hiring Analyst – Pharmacovigilance (0–2 Years)
If you are planning to build a career in pharmacovigilance (drug safety), this is a great opportunity to get started. Elanco has announced openings for the role of Analyst – PV in Bangalore, and candidates with 0 to 2 years of experience can apply.
This role is ideal for freshers and early-career professionals from pharmacy, life sciences, or veterinary backgrounds who are interested in adverse event reporting and drug safety operations.
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🏢 About Hiring Organization
Elanco is a global animal health company that focuses on improving the health of pets and farm animals. The company develops products and solutions that help prevent and treat diseases while supporting sustainable food production.
Elanco is known for its positive work culture, learning opportunities, and focus on innovation. Employees get a chance to work on global projects and gain exposure to international pharmacovigilance systems.
📌 Job Overview
The Analyst – Pharmacovigilance (PV) role mainly involves handling adverse event case processing, monitoring safety data, and supporting global pharmacovigilance activities.
This is a full-time position based in Bangalore, where you will work as part of a team responsible for maintaining drug safety data and ensuring compliance with regulatory requirements.
💼 Job Details
- Company: Elanco
- Job Role: Analyst – PV
- Location: Bangalore, India
- Experience: 0–2 Years
- Department: Pharmacovigilance / Drug Safety
- Employment Type: Full-Time
- Application Deadline: June 3, 2026
💼 Key Responsibilities
In this role, you will work on different pharmacovigilance activities. Your responsibilities will mainly include:
📊 Adverse Event Case Processing
- Entering adverse event data into PV databases
- Performing seriousness and causality assessments
- Reviewing case details to ensure accuracy and completeness
- Validating information against source documents
- Identifying missing data and following up if needed
- Ensuring cases are submitted within timelines
- Participating in team meetings and case discussions
🌍 Global Pharmacovigilance Support
- Supporting international drug safety processes
- Managing safety-related email inboxes
- Assisting in submission of Individual Case Safety Reports (ICSRs)
- Coordinating with global PV teams and stakeholders
🤝 Customer & Internal Collaboration
- Communicating with internal teams, affiliates, and external partners
- Coordinating with customer response and legal teams when required
- Maintaining confidentiality of sensitive data
- Supporting communication related to drug safety activities
🎓 Qualification Criteria
Candidates with the following qualifications can apply:
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Biotechnology / Microbiology / Biochemistry
👉 Freshers are eligible, and candidates with up to 2 years of experience in pharmacovigilance are also encouraged to apply.
✅ Skills you have
To perform well in this role, you should have:
- Basic knowledge of medical and clinical terminology
- Understanding of adverse event reporting
- Good communication skills
- Strong attention to detail
- Ability to learn quickly and adapt
- Teamwork and coordination skills
Having basic knowledge of pharmacovigilance processes will be helpful but is not mandatory for freshers.
📊 Role detail Insight
The Analyst – PV role is a backend, process-driven job that focuses on managing drug safety data. You will mainly be working on systems, reviewing reports, and making sure all safety information is correct.
Pharmacovigilance is an important part of the pharma industry because it ensures that medicines are safe even after they are available in the market. Every reported side effect needs to be documented properly.
If you are someone who enjoys working with data, analyzing information, and maintaining accuracy, this role can suit you well.
👤 Applicable for
This opportunity is ideal for:
- Freshers from pharmacy, life sciences, or veterinary backgrounds
- Candidates interested in pharmacovigilance or drug safety careers
- Individuals who prefer structured, office-based roles
- Those who want to work in a global healthcare environment
🚀 Growth Opportunities
Starting as a PV Analyst can open many career opportunities in the future. With experience, you can move into roles such as:
- Drug Safety Associate
- Pharmacovigilance Specialist
- Medical Reviewer
- Signal Detection Expert
- Regulatory Affairs roles
Since drug safety is a mandatory requirement globally, this field offers strong career stability and growth.
💰 Pay Expectation
Based on industry standards in Bangalore:
💵 ₹3.5 LPA – ₹6 LPA
The final salary depends on your experience, skills, and interview performance.
🌟 Why Join Elanco?
Here are a few reasons why this role is a good opportunity:
- ✅ Work with a global animal health company
- ✅ Exposure to international pharmacovigilance systems
- ✅ Strong learning and development environment
- ✅ Inclusive and supportive work culture
- ✅ Career growth in drug safety and regulatory fields
💡 Advance Tips for Applicants
If you are planning to apply for this role, here are some simple tips:
- Prepare a clear and updated resume
- Highlight any knowledge of pharmacovigilance or clinical research
- Learn basic concepts like:
- Adverse Drug Reactions (ADR)
- ICSR
- Drug safety reporting
- Improve your Excel and computer skills
- Be confident and show your interest in pharmacovigilance
📝 How to Apply
Interested candidates can apply through the official Elanco careers page:
🚀 Application link🔗 Explore Similar Opportunities
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📚 Career Guide
- How to start career in Pharmcovigilance guide
- Guide on how to create resume for fresher
- Best career option after B.pharm
- Top 25 question asked in PV interview
📝 Final Thoughts
The Analyst – PV role at Elanco is a great starting point for freshers who want to enter the pharmacovigilance field. It provides practical exposure to adverse event processing, global safety systems, and regulatory workflows.
If you are serious about building a career in drug safety, this role can give you the right foundation and help you grow in the pharmaceutical industry.
