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Specialist Pharmacovigilance

1-3 years
Not Disclosed
10 July 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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 – Cencora, Noida

Location: Noida, India
Job Type: Full-time
Salary/Compensation: Not specified


Job Summary

Cencora is seeking a Specialist Pharmacovigilance to support literature screening, safety data management, and ICSR processing. This role is key to ensuring drug safety compliance and involves managing safety reports, performing duplicate checks, preparing standard reporting forms (CIOMS I/MedWatch), and acting as a liaison with client project teams.


Responsibilities

  • Screen scientific literature using internal search mechanisms and external tools/providers.

  • Classify safety-relevant publications and manage the internal literature ordering process.

  • Perform data entry of literature reports into the safety database.

  • Prepare standard reporting forms such as CIOMS I, MedWatch, and XML files.

  • Complete and document cases with high accuracy.

  • Download, review, and share client-specific ICSRs from EMA’s Medical Literature Monitoring (MLM) service.

  • Perform duplicate searches of literature cases against updated MLM information.

  • Serve as the primary contact for client/project management.

  • Undertake additional pharmacovigilance tasks across service lines as required.


Required Skills & Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related fields.

  • Experience in literature screening, ICSR processing, and safety database management.

  • Knowledge of CIOMS I, MedWatch forms, and XML safety reporting.

  • Familiarity with EMA’s MLM service and medical literature monitoring practices.

  • Strong organizational skills and attention to detail.

  • Effective communication and project management skills.


Perks & Benefits

  • Competitive compensation aligned with industry standards.

  • Opportunity to work with a global healthcare and consulting leader.

  • Equal employment opportunity and inclusive work culture.

  • Career growth through diverse pharmacovigilance projects.


Company Description

Cencora, through its affiliate PharmaLex India Private Limited, is a global healthcare and consulting leader, committed to creating healthier futures. With expertise in pharmacovigilance, drug safety, and regulatory affairs, Cencora supports the life sciences industry worldwide, driving innovation and compliance across clinical and post-marketing drug safety operations.


Work Mode: On-site (Noida, India)


Call-to-Action

Take your pharmacovigilance career to the next level with Cencora. Apply now for the Specialist Pharmacovigilance role in Noida and contribute to global drug safety excellence.