Cencora Hiring for Senior Specialist- Pharmacovigilance Role: PV Jobs 2026

ByPharma Hiring Hub

Cencora, a global healthcare services and pharmaceutical solutions organization, is hiring for the role of Senior Specialist – Pharmacovigilance at its Noida location. This opportunity is suitable for candidates with a B.Pharm or M.Pharm degree and 2 years of hands‑on experience in pharmacovigilance and ICSR case processing.

The role focuses on end‑to‑end safety case management, regulatory compliance, and supporting global pharmacovigilance operations within a structured and regulated environment. Candidates will work closely with cross‑functional safety teams to ensure accurate, timely, and compliant handling of adverse event data.

This position offers strong exposure to global PV processes, safety systems, and long‑term career growth within Cencora’s patient safety and drug safety operations.

Cencora Pv jobs

Job Overview

  • Position: Senior Specialist- Pharmacovigilance
  • Department: PV
  • Location: Noida, India
  • Experience: 2+ Years
  • Qualification: B.Pharm, M.pharm
  • Job Type: Full-Time
  • Last Date to apply: 12 May2026

Key Responsibilities – Senior Specialist- Pharmacovigilance

  • Literature Screening & Monitoring
    • Screen scientific and biomedical literature using internal search systems and approved external tools or service providers.
    • Track and manage the internal literature ordering process to ensure timely retrieval of required publications.
  • Safety Literature Classification & Data Entry
    • Classify safety‑relevant publications according to established pharmacovigilance criteria.
    • Perform accurate data entry of literature cases into the pharmacovigilance safety database.
  • ICSR Processing & Documentation
    • Prepare standard regulatory reporting forms such as CIOMS I, MedWatch forms, and relevant XML files.
    • Complete case processing activities including case completion, review, and documentation.
  • EMA MLM & Duplicate Check Activities
    • Download, review, and distribute client‑specific ICSRs from the EMA Medical Literature Monitoring (MLM) service.
    • Perform duplicate searches for literature cases using updated information available in the EMA MLM system.
  • Client & Project Coordination
    • Act as the primary point of contact for clients and project management teams regarding safety literature and ICSR activities.
  • Cross‑Service Support
    • Support additional pharmacovigilance service lines and related tasks, as required, in alignment with skills, training, and qualifications

Required Skills & Qualifications

  • Educational Background: Bachelor’s or University degree in Life Sciences, Pharmacy, or a related scientific discipline with 2+ Years of experience in PV ICSR
  • Communication Skills:Strong written and verbal communication skills with a good command of the English language.
  • Organizational & Problem‑Solving Skills: Effective organizational, planning, and problem‑solving abilities to manage multiple study tasks.
  • Time & Financial Management:Capable of managing time, priorities, and site‑level financial activities efficiently.
  • Professional Relationships: Ability to establish and maintain effective working relationships with study sites, coworkers, managers, and clients.

Why Join Cencora?

  • Global Healthcare Organization
  • Join Cencora, a leading global healthcare services company supporting pharmaceutical and biotech organizations across clinical research, pharmacovigilance, and regulatory operations.
  • Strong Pharmacovigilance Exposure
  • Gain hands‑on experience in ICSR processing, literature monitoring, regulatory reporting, and safety database management, working within a structured global PV framework.
  • Career Growth in Drug Safety
  • The Senior Specialist role offers opportunities to deepen expertise in safety operations, compliance activities, and client‑focused pharmacovigilance services, supporting long‑term career progression.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ-Senior Specialist- Pharmacovigilance

1. Who can apply for the Senior Specialist – Pharmacovigilance role at Cencora?

Candidates with a B.Pharm or M.Pharm degree and at least 2 years of experience in pharmacovigilance and ICSR case processing are eligible to apply.

2. What type of pharmacovigilance activities will I handle in this role?

You will manage literature screening, ICSR processing, duplicate checks, safety data entry, regulatory reporting, and documentation aligned with global PV requirements.

3. Is this role focused on literature monitoring?

Yes. The role includes screening scientific literature, classifying safety‑relevant publications, and working with the EMA Medical Literature Monitoring (MLM) system.

4. What safety systems or tools will I work with?

You will work with pharmacovigilance safety databases, internal search systems, EMA MLM services, and tools used for CIOMS I, MedWatch, and XML reporting.

5. Will I be responsible for client interactions?

Yes. You will act as a primary point of contact for assigned clients and project management teams for literature and ICSR‑related activities.

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