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Pharmacovigilance Specialist – Case Processing

0-2 years
3-5 LPA
10 Nov. 26, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate 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

Pharmacovigilance Specialist – Case Processing | Cencora | Noida, India

Job ID: R2517900
Category: Consulting
Posted On: 26 November 2025
Experience Required: Fresher


About Cencora

Cencora is a global healthcare organization driven by the mission to create healthier futures for people and animals worldwide. Every team member plays a vital role in delivering high-quality services that strengthen patient safety and support medical innovation. If you want to build a meaningful career at the center of global health, this opportunity offers a strong foundation for growth.


Role Overview

The Specialist – Case Processing will support end-to-end Individual Case Safety Report (ICSR) activities, ensuring compliance with global pharmacovigilance regulations. This position is well-suited for freshers seeking to begin a career in drug safety, case management, and regulatory reporting.


Key Responsibilities

Case Intake, Review, and Validation

  • Perform triage and initial validity assessment of spontaneous, clinical trial, literature, and health authority cases.

  • Enter case information into the pharmacovigilance database with high accuracy.

  • Conduct preliminary ICSR assessment based on project requirements.

Regulatory Reporting Activities

  • Evaluate the need for expedited reporting to global Health Authorities and partners.

  • Track and ensure compliance with regulatory reporting timelines.

  • Prepare standard reporting formats, including CIOMS I, MedWatch, and XML submissions.

  • Prepare and dispatch follow-up information requests as needed.

  • Submit ICSRs to Health Authorities and external partners.

Quality and Documentation

  • Perform quality checks of ICSRs to ensure alignment with industry standards and client expectations.

  • Maintain comprehensive case documentation for audit readiness.

  • Support ICSR search and retrieval from EVWEB and perform company vs. non-company case assessments.

Collaboration and Team Support

  • Mentor and support new team members by providing process guidance and encouraging skill development.

  • Collaborate effectively within the assigned project and escalate operational queries to supervisors as required.

  • Contribute to a culture of accuracy, consistency, and continual improvement across pharmacovigilance operations.


What Cencora Offers

Benefits vary by country and follow local market practices. Eligibility and effective dates may differ for team members covered under country-specific guidelines or collective bargaining agreements.


Employment Type

Full-Time
Affiliated Company: PharmaLex India Private Limited