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Associate Manager - Pv Case Processing

4-7 years
Not Disclosed
10 Dec. 5, 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

Associate Manager – Pharmacovigilance (PV) Case Processing

Location: Bangalore, India
Employment Type: Full-Time
Company: Elanco Animal Health

Elanco (NYSE: ELAN) is a global leader in animal health, committed to developing innovative solutions to prevent, manage, and treat diseases in farm animals and companion animals. Built on the vision of Food and Companionship Enriching Life, Elanco continues to advance scientific excellence and operational integrity across the industry.

As part of its expanding global pharmacovigilance operations, Elanco invites applications for the role of Associate Manager – PV Case Processing. This position is ideal for professionals seeking to grow their expertise in global safety, regulatory compliance, and case management within a diverse and inclusive workplace.


Role Overview

The Associate Manager – PV Case Processing will be responsible for the accurate assessment, processing, and regulatory submission of adverse event reports in accordance with global pharmacovigilance guidelines. The role demands strong analytical skills, adherence to compliance standards, and effective cross-functional communication to support both internal teams and external partners.


Key Responsibilities

  • Ensure prompt identification, escalation, and resolution of issues that may impact case submission timelines.

  • Process and submit adverse event and product complaint cases within established global and internal deadlines.

  • Validate data entry with high accuracy by cross-checking information against source documents, call notes, and follow-up materials.

  • Conduct effective written and verbal communication to obtain follow-up information from external stakeholders.

  • Stay updated on evolving global pharmacovigilance requirements, guidelines, and best practices.

  • Maintain confidentiality and ensure secure handling of sensitive company and safety-related data.


Minimum Qualifications

  • Veterinary degree (equivalent to US DVM) with or without prior PV experience, OR

  • Bachelor’s degree in Pharmacy, Life Sciences, or related fields with 4–7 years of pharmacovigilance experience.


Preferred Qualifications

  • Strong foundational knowledge of medical terminology and clinical concepts relevant to adverse event evaluation.

  • Expertise in data entry accuracy, validation, and quality review of case-related documentation.

  • Ability to build effective working relationships with colleagues, managers, and cross-functional partners.

  • Demonstrated willingness to learn and adapt within evolving safety and regulatory environments.

  • Strong teamwork skills with the ability to contribute to shared operational goals.

  • Flexibility to manage extended work hours during peak workloads.


Additional Details

  • Travel Requirement: 0%

  • Work Location: Bangalore, India

Elanco is committed to fostering diversity, equity, and inclusion. Candidates who may not meet every listed qualification but believe they can contribute meaningfully to the role are encouraged to apply.

Elanco is an Equal Employment Opportunity/Affirmative Action employer and does not discriminate based on race, color, age, religion, gender, sexual orientation, gender identity, disability, national origin, or protected veteran status.