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Analyst - R&D

0-1 years
Not Disclosed
10 Sept. 22, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Analyst – R&D (Pharmacovigilance Case Processing)

Location: Bangalore, India
Employment Type: Full-time
Requisition ID: R0023343
Posted: 3 days ago
Travel: 0%


Company Overview – Elanco

Elanco (NYSE: ELAN) is a global leader in animal health, dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.

  • Vision: Food and Companionship Enriching Life

  • Purpose: Go Beyond for Animals, Customers, Society, and Our People

  • Culture: Diverse and inclusive work environment fostering innovation, creativity, and career growth


Role Overview

The Analyst – R&D in pharmacovigilance is responsible for managing adverse event reports (AEs), ensuring data accuracy, and maintaining compliance with global pharmacovigilance regulations and timelines. The role includes data entry, assessing seriousness and causality, and preparing cases for regulatory submission.


Key Responsibilities

  • Perform data entry for adverse event reports in the pharmacovigilance (PV) database.

  • Assess seriousness and causality of adverse event reports.

  • Identify issues in case processing that may delay submissions and escalate them appropriately.

  • Develop a strong understanding of pharmacovigilance regulations.

  • Comply with internal and external timelines for adverse event and product complaint processing and submission.


Required Qualifications & Skills

  • Education: Bachelor’s or Master’s degree in a relevant field

  • Experience: 0–1 year in pharmacovigilance or related area

  • Basic knowledge of medical terminologies and ability to understand common terms used in pharmacovigilance and adverse event reporting


Preferred Qualifications / Competitive Edge

  • Effective verbal and written communication skills to liaise with internal and external stakeholders

  • Ability to work on multiple products and manage priorities effectively

  • Capability to establish and maintain working relationships with coworkers, managers, and stakeholders

  • Understanding of global and local regulatory requirements and ability to comply with them


Company Commitment

  • Elanco promotes a diverse and inclusive workplace. Candidates who do not meet every requirement are encouraged to apply.

  • Equal Employment Opportunity (EEO): Elanco does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity or expression, national origin, veteran status, disability, or any other legally protected status.