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Analyst - R&D

0-1 years
Not Disclosed
10 Nov. 1, 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

Position: Analyst – R&D (Pharmacovigilance Case Processing)

Company: Elanco (NYSE: ELAN)
Location: Bangalore, India
Employment Type: Full-time
Job ID: R0023343
Posted: 25 Days Ago


About Elanco

Elanco is a global leader in animal health, dedicated to innovation and developing products and services that prevent and treat diseases in farm animals and pets. Guided by our vision — “Food and Companionship Enriching Life” — we strive to go beyond for animals, customers, society, and our people.

We foster a diverse and inclusive workplace, encouraging creativity, collaboration, and continuous learning to empower employees to reach new professional heights.


Role Overview

The Analyst – R&D (PV Case Processing) is responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global pharmacovigilance regulations and timelines. The role requires data entry, seriousness and causality assessment, and quality control of case submissions to regulatory authorities.


Key Responsibilities

  • Perform data entry of adverse event reports in the PV database.

  • Conduct seriousness and causality assessments of reported events.

  • Ensure completeness, accuracy, and compliance of case data for regulatory submissions.

  • Identify and escalate potential delays or processing issues to management.

  • Adhere to internal and external timelines for adverse event and product complaint management.

  • Develop a thorough understanding of pharmacovigilance processes and regulations.


Required Qualifications

  • Bachelor’s or Master’s degree in Life Sciences or a related field.

  • 0–1 year of relevant experience.

  • Basic understanding of medical terminology, pharmacovigilance, and adverse event reporting.


Preferred Qualifications

  • Strong verbal and written communication skills.

  • Ability to manage multiple tasks and prioritize effectively.

  • Team-oriented mindset with the ability to build strong professional relationships.

  • Awareness of global and local regulatory requirements.


Additional Information

  • Travel: None (0%)

  • Location: Bangalore, India

  • Elanco encourages applications from candidates of all backgrounds, even if they do not meet every listed qualification.