Medical Reviewer – Pharmacovigilance Case Processing
Location: Noida, Uttar Pradesh, India
Employment Type: Full-Time
Category: Consulting
Job ID: R2522052
Posted Date: December 17, 2025
Industry: Pharmacovigilance | Drug Safety | Life Sciences
Job Overview
Cencora is seeking an experienced Medical Reviewer – Case Processing to support global pharmacovigilance operations through expert medical assessment and review of Individual Case Safety Reports (ICSRs). This role plays a critical part in ensuring high-quality medical evaluation, regulatory compliance, and patient safety across multiple therapeutic areas.
The position is ideal for medical professionals with extensive experience in drug safety, medical review workflows, and global regulatory standards.
Key Responsibilities
Medical Review & Case Assessment
Perform initial medical assessment and review of ICSRs within the safety database.
Evaluate adverse events captured from source documents, ensuring accurate assessment of:
Seriousness criteria
MedDRA coding
Suspect and concomitant medications
Laboratory data and medical history
Product labelling and causality
Review and finalize case narratives, including providing company causality comments.
Quality Oversight & Compliance
Respond to medical queries and comments raised by Case Owners within the safety database.
Ensure appropriate documentation of medical review decisions within defined workflows.
Maintain strong working knowledge of global pharmacovigilance regulations, including ICH, EMA, FDA, GVP, and GCP guidelines.
Support internal and external audits and regulatory inspections as required.
Training & Stakeholder Collaboration
Train and mentor pharmacovigilance associates on event capturing standards and PV conventions.
Escalate complex or high-risk safety cases to the Team Lead or Line Manager in a timely manner.
Actively participate in internal project meetings and cross-functional discussions.
Perform additional drug safety–related activities as assigned by management.
Qualifications
Essential: Degree in Medicine (MBBS or equivalent)
Preferred: Postgraduate qualification in any medical discipline (advantageous but not mandatory)
Experience Required
Minimum 8 years of hands-on experience in Pharmacovigilance and Drug Safety, including medical review of ICSRs and regulatory case processing
Skills & Competencies
Strong expertise in medical assessment, causality evaluation, and safety data interpretation
Excellent understanding of global PV regulations and safety databases
Strong interpersonal and organizational skills with the ability to work collaboratively
High level of accountability, professionalism, and ability to perform under pressure
Service-oriented mindset with prior exposure to pharmaceutical, CRO, or life sciences environments
Excellent written and spoken English communication skills
What Cencora Offers
Competitive compensation aligned with local market practices
Exposure to global pharmacovigilance programs and multinational clients
Inclusive, diverse, and ethics-driven work culture
Career development within a leading global healthcare organization
Affiliated Entity
PharmaLex India Private Limited (a Cencora company)
Equal Employment Opportunity Statement
Cencora is committed to providing equal employment opportunities without discrimination based on race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or any other legally protected status. Reasonable accommodations are available for individuals with disabilities throughout the employment process, in accordance with applicable laws.
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