Cencora PharmaLex Hiring Pharmacovigilance Jobs in Noida

Apply for Pharmacovigilance Specialist at Cencora, Noida. Life science graduates with PV experience preferred. Full-time role.

Cencora is hiring a Pharmacovigilance Specialist to support epidemiology and risk management functions. This role suits candidates with strong PV case processing skills who want to contribute to global drug safety operations. The position offers structured responsibilities, exposure to regulatory workflows, and the opportunity to support high‑quality safety data management.

Company Overview

Cencora is a global leader in healthcare solutions, advancing safety and compliance for life sciences organizations worldwide. Through its affiliate PharmaLex India, the company delivers regulatory, pharmacovigilance, and consulting services that enhance product safety, compliance, and patient outcomes. The Noida team supports global partners and health authorities with high‑integrity safety reporting and risk management practices.

Job Role & Responsibilities

The Pharmacovigilance Specialist is responsible for case processing, quality checks, and safety reporting tasks across spontaneous, clinical trial, literature, and regulatory cases. Core responsibilities include:

• Performing triage and initial validity review of ICSRs.
• Entering case data into the PV database and completing ICSR documentation.
• Evaluating cases for expedited reporting requirements to health authorities and partners.
• Preparing CIOMS I / MedWatch forms and XML reports.
• Preparing and sending follow‑up requests to sites or reporters.
• Submitting ICSRs to global health authorities and client partners.
• Conducting rigorous quality checks of ICSRs to maintain compliance and data integrity.
• Retrieving ICSRs from EVWEB and performing company/non‑company case assessments.
• Supporting case completion and ensuring documentation accuracy.
• Mentoring new joiners and assisting them in learning internal processes.
• Completing additional tasks assigned by the supervisor as required.

Eligibility / Qualifications

• Life sciences background (Pharmacy, Nursing, Biotechnology, Medical, Dentistry, or related fields).
• Strong experience in pharmacovigilance case processing and safety reporting.
• Knowledge of ICSR workflows, regulatory reporting timelines, and global PV guidelines.
• Experience with EVWEB, safety databases, and standard safety reporting formats.
• Strong communication, documentation, and quality review skills.
• Ability to work independently and manage time‑sensitive tasks.

Location & Salary

• Location: Noida, India
• Role Type: Full‑time
• Work Mode: Office-based (Consulting Division)
• Salary and benefits aligned to Cencora’s local market structure.

Application Process

Interested candidates can apply directly through the official Cencora careers portal:

🔗 Apply Here: https://careers.cencora.com/us/en/job/CHKCENUSR2519675EXTERNALENUS/Specialist-Pharmacovigilance-Epidemiology-Risk-Management

Summary Table

FAQs

1. What qualifications are required for this role?
A degree in life sciences (Pharmacy, Nursing, Biotechnology, Medical, Dentistry) with prior PV experience is preferred.

2. Does this role involve ICSR case processing?
Yes, case processing, triage, documentation, and reporting are core responsibilities.

3. Is experience in EVWEB or safety databases required?
Familiarity with EVWEB and standard reporting formats (CIOMS, MedWatch) is highly beneficial.

4. Is this a full‑time role?
Yes, it is a full‑time consulting position based in Noida.

5. How do I apply?
You can apply through the official Cencora careers link provided above.

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