Cencora – Senior Specialist, Pharmacovigilance | Noida, India | Drug Safety
Company: Cencora (Affiliated: PharmaLex India Private Limited)
Location: Noida, India
Job Type: Full-Time
Work Mode: On-site / Hybrid (project-dependent)
Experience: 2+ Years (Pharmacovigilance / Drug Safety)
Qualification: Life Sciences Degree
Compensation: Not disclosed in the job description
Pharmacovigilance jobs in Noida are rapidly growing, especially roles focused on ICSR processing, medical literature review, and regulatory safety reporting, making this an excellent opportunity in drug safety careers.
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Job Summary
Cencora is hiring a Senior Specialist – Pharmacovigilance to support medical literature monitoring, ICSR processing, and safety data management. This role plays a key part in drug safety surveillance and regulatory compliance, ensuring accurate capture and reporting of adverse events from scientific literature.
You will work on literature screening, case processing, and safety database management, making this a strong opportunity for professionals building expertise in pharmacovigilance operations and regulatory safety workflows.
This role is ideal for candidates aiming to grow in:
Pharmacovigilance (PV)
Drug Safety Case Processing
Medical Literature Monitoring (MLM)
Regulatory Safety Reporting
Key Responsibilities
Medical Literature Monitoring (MLM)
Screen scientific literature using internal tools and external databases
Identify and classify safety-relevant publications
Manage literature ordering and tracking processes
ICSR Case Processing & Safety Data Entry
Perform data entry of literature cases into safety databases
Download and review ICSRs from EMA Medical Literature Monitoring (MLM) service
Conduct duplicate checks and ensure data accuracy
Regulatory Reporting & Documentation
Prepare standard safety reporting forms:
CIOMS I Forms
MedWatch Forms
XML safety files
Ensure complete and compliant case documentation
Pharmacovigilance Operations
Support case completion and workflow management
Maintain compliance with global drug safety regulations
Collaborate with internal teams and external clients
Client & Project Coordination
Act as primary contact for client/project-related communication
Support delivery across pharmacovigilance service lines
Ensure high-quality service and client satisfaction
Required Skills & Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
Minimum 2+ years of pharmacovigilance experience
Basic understanding of:
Pharmacovigilance processes
ICSR case processing
Medical literature review
Knowledge of:
Global drug safety regulations
Adverse event reporting standards
Strong communication and presentation skills
Attention to detail and ability to manage multiple tasks
Preferred Skills (High-Impact SEO Keywords):
ICSR Processing & Case Management
Medical Literature Monitoring (MLM)
MedDRA Coding
CIOMS / MedWatch Reporting
Pharmacovigilance Databases (Argus, ARISg, etc.)
Regulatory Compliance & Safety Reporting
Perks & Benefits
Opportunity to work with a global pharmacovigilance consulting organization
Exposure to EMA and global safety reporting systems
Career growth in drug safety and regulatory affairs
Collaborative and client-focused work environment
Diverse international project exposure
About the Company
Cencora is a global healthcare solutions provider specializing in pharmaceutical services, consulting, and drug safety operations. Through its affiliate PharmaLex, the company delivers expertise in pharmacovigilance, regulatory affairs, and clinical development, supporting global life sciences organizations.
Why This Role is Important in Pharma Careers
The Senior Specialist – Pharmacovigilance role is a critical part of drug safety operations, ensuring accurate identification and reporting of adverse events from global literature sources.
This role provides exposure to:
EMA Medical Literature Monitoring (MLM) systems
ICSR processing workflows
Regulatory safety documentation
Global pharmacovigilance compliance
Career growth opportunities include:
Drug Safety Associate / PV Specialist
Pharmacovigilance Scientist
Safety Data Analyst
Regulatory Safety Specialist
Application Process
Apply through the official Cencora careers portal
Highlight experience in:
Pharmacovigilance
ICSR processing
Medical literature review
Use keywords:
Drug Safety
MedDRA
CIOMS
Pharmacovigilance
Call to Action
If you want to build a strong career in pharmacovigilance, drug safety, and regulatory compliance, this is your opportunity.
Apply now and grow in the global drug safety ecosystem with Cencora 🚀
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