Analyst – Pharmacovigilance (PV) | Elanco
Job Details
Job Title: Analyst – Pharmacovigilance (PV)
Company: Elanco
Job ID (Req ID): R0025509
Location: Bangalore, Karnataka, India
Job Type: Full-time
Experience Required: 0–2 years
Posted: 3 days ago
Estimated Salary Package (Market Standard): ₹4.5 – ₹7.5 LPA (official salary not disclosed)
About the Company
Elanco is a global leader in animal health, dedicated to developing innovative products and services for the prevention and treatment of diseases in farm animals and pets. Operating worldwide, Elanco focuses on improving animal health while fostering an inclusive and collaborative workplace.
Job Purpose
The Analyst – Pharmacovigilance (PV) will be responsible for adverse event case processing, pharmacovigilance data management, regulatory submissions, and global PV support, ensuring compliance with global pharmacovigilance regulations and internal quality standards.
Key Responsibilities
1. Adverse Event Case Processing
Perform data entry of adverse event (AE) reports into the PV database.
Assess case seriousness, causality, and reportability.
Validate data against source documents and call notes.
Review case information for completeness, accuracy, and quality.
Determine follow-up information required for incomplete cases.
Ensure cases are submission-ready for regulatory authorities.
Meet productivity, quality, and compliance targets.
Escalate issues that may delay case processing or submissions.
Participate in team meetings and support assigned PV activities.
2. Global Pharmacovigilance (GPV) Support
Stay updated with global pharmacovigilance regulations and industry practices.
Support internal teams on GPV-related activities.
Collaborate with global PV colleagues.
Manage the global adverse events mailbox.
Perform regulatory submissions of Individual Case Safety Reports (ICSRs).
3. Internal & External Collaboration
Communicate effectively with affiliate offices, call centers, legal teams, and customer support groups.
Maintain confidentiality of company and patient information.
Ensure confidentiality agreements are in place before sharing sensitive information.
Support cross-functional teams in pharmacovigilance activities.
Required Qualifications
0–2 years of experience in Pharmacovigilance.
Basic understanding of PV Case Processing and Study Literature.
Knowledge of medical terminology related to adverse event reporting.
Good communication and interpersonal skills.
Strong learning agility and attention to detail.
Preferred Qualifications
Experience in Pharmacovigilance (PV) Case Processing.
Familiarity with Individual Case Safety Reports (ICSRs).
Knowledge of global pharmacovigilance regulations.
Experience in regulatory submissions is an advantage.
Preferred Skills
Pharmacovigilance (PV) Case Processing.
Adverse Event (AE) reporting.
Individual Case Safety Reports (ICSRs).
Seriousness and causality assessment.
Medical terminology.
Regulatory compliance.
Data entry and quality review.
Case validation and follow-up.
Study literature review.
Microsoft Office (Word, Excel, Outlook).
Communication and teamwork.
Attention to detail and time management.
One-Line Experience
Candidates with 0–2 years of experience in Pharmacovigilance, adverse event case processing, ICSR management, or drug safety operations within the pharmaceutical, CRO, or healthcare industry are preferred.
Estimated Salary Package (Market Standard)
Freshers (0–1 Year): ₹4.5 – ₹6.0 LPA
Experienced (1–2 Years): ₹6.0 – ₹7.5 LPA
Note: The official salary has not been disclosed by Elanco.
Why Join Elanco?
Work with a globally recognized leader in animal health.
Gain hands-on experience in global pharmacovigilance and drug safety operations.
Exposure to international regulatory compliance and adverse event reporting.
Collaborative and inclusive work culture with strong learning opportunities.
Excellent career growth in Pharmacovigilance, Drug Safety, and Regulatory Affairs.
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