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Specialist, Pharmacovigilance, Icsr - Hyderabad

5-8 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time Hybrid 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

Specialist, Pharmacovigilance, ICSR – Hyderabad, India

Location: Hyderabad, Andhra Pradesh, India
Job Type: Full-Time / Hybrid Work
Job ID: R-045354
Function: Product Safety
Sub-Function: Pharmacovigilance
Category: Experienced Scientist, Pharmacovigilance (ST5)


About Johnson & Johnson

At Johnson & Johnson, we are committed to transforming healthcare through innovation. Leveraging expertise in Innovative Medicine and MedTech, we aim to prevent, treat, and cure complex diseases while making treatments smarter, safer, and more patient-centric. Join a global team delivering the breakthroughs of tomorrow. Learn more at jnj.com.


Position Overview

The Specialist, Pharmacovigilance, ICSR plays a critical role in global case management by designing, implementing, and sustaining innovative processes and technology-driven solutions. This role combines scientific expertise with operational excellence to enhance efficiency, compliance, and data quality in patient safety reporting.

This position is ideal for candidates with 5–8 years of experience in pharmacovigilance or regulated operations who are ready to lead ICSR process improvements and automation initiatives in a dynamic, global environment.


Key Responsibilities

  • Lead and support the development, deployment, and continuous improvement of ICSR capabilities, including automation, AI-driven, and data-enhanced solutions.

  • Collaborate with Case Management and cross-functional teams to ensure operational readiness, adoption, and regulatory compliance of new tools and processes.

  • Implement governance, training, and performance monitoring frameworks to maintain inspection-ready operations.

  • Apply pharmacovigilance expertise to assess data accuracy, compliance, and alignment with global PV standards.

  • Partner with system and process owners to identify gaps, recommend corrective actions, and implement sustainable solutions.

  • Support core case-management operations, providing input and validation for protocol-related or capability-linked activities.

  • Design and execute structured case-testing scenarios, including creation of realistic ICSR cases, detailed test scripts, and validation steps to ensure system integrity.


Behavioral Competencies

  • Ability to work independently and proactively in a remote, cross-regional environment.

  • Strong problem-solving skills, with the ability to identify issues, propose solutions, and escalate appropriately.

  • Collaborative team spirit, with effective communication and respect for colleagues across sites and time zones.

  • High professionalism, accountability, and a consistent focus on quality and regulatory compliance.

  • Adaptable, solution-oriented, and capable of navigating ambiguity and shifting priorities.


Required Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related field.

  • 5–8 years of experience in pharmacovigilance, ICSR case management, or regulated operations.

  • Deep understanding of the ICSR lifecycle (intake, processing, reporting) and PV concepts, including seriousness, causality, expectedness, and MedDRA coding.

  • Experience contributing to process improvement, automation, or workflow optimization in a regulated environment.

  • Experience designing, writing, and executing test scripts or case-testing scenarios.

  • Strong analytical, collaboration, and communication skills.

  • Fluency in English (written and spoken).


Preferred Qualifications

  • Experience with PV safety systems such as ArisGlobal LifeSphere, Oracle Argus, or similar platforms.

  • Familiarity with automation, AI, and innovation tools (e.g., GenAI).

  • Understanding of metrics, KPIs, and continuous improvement methodologies.

  • Demonstrated ability to work effectively in a dynamic, global environment.


Key Skills

Required: Pharmacovigilance, ICSR Management, Clinical Operations, Quality Control (QC), Regulatory Compliance, Root Cause Analysis (RCA), Safety Investigations, Data Accuracy, Report Writing.

Preferred: Process Optimization, Cross-Functional Collaboration, Technologically Savvy, Coaching, Performance Measurement, Analytical Reasoning.