Job Title: Medical Reviewer – Case Processing
Location: Noida, India
Employment Type: Full-Time
Category: Consulting / Pharmacovigilance
Experience Required: Minimum 8 years in Pharmacovigilance and Drug Safety
Cencora is a global leader in healthcare solutions, committed to creating healthier futures for people and animals worldwide. Our mission is centered on advancing healthcare through innovation, collaboration, and scientific rigor. As part of our team, you will contribute to the pharmacovigilance and drug safety processes that ensure patient safety and regulatory compliance across multiple therapeutic areas.
We are seeking an experienced Medical Reviewer – Case Processing to join our Noida team. The role involves performing medical review of Individual Case Safety Reports (ICSRs), ensuring accuracy, regulatory compliance, and high-quality documentation in the safety database. The position also includes mentoring PV associates, escalating complex cases, and participating in audits and inspections.
Conduct initial assessment and medical review of ICSRs in the safety database.
Verify adverse event coding, seriousness criteria, suspect drugs, concomitant medications, lab data, medical history, labeling, causality, and narratives.
Provide Company Causality Comments and respond to queries from Case Owners in the safety database.
Train and mentor PV associates on adverse event capturing and pharmacovigilance conventions.
Maintain up-to-date knowledge of products and safety profiles across therapeutic areas.
Escalate complex case issues to Team Lead or Line Manager.
Document follow-up requirements and case review comments accurately in the safety database.
Maintain strong knowledge of databases, regulations, SOPs, and pharmacovigilance guidelines (GVP, GCP, ICH, EMA, FDA).
Actively participate in internal project meetings, audits, and inspections.
Perform any additional drug safety activities assigned by management.
Medical degree (MBBS required). Postgraduate degree in any discipline is an advantage but not mandatory.
Minimum 8 years of experience in Pharmacovigilance and Drug Safety.
Strong understanding of GVP, GCP, ICH, EMA, and FDA guidelines.
Excellent interpersonal and organizational skills for effective teamwork.
High sense of responsibility, dedication, and ability to work under pressure.
Service-oriented mindset with previous exposure to pharma or life sciences preferred.
Fluent in English, both spoken and written.
Strong analytical thinking and attention to detail for regulatory compliance.
Be part of a global, innovative healthcare organization with a focus on patient safety and regulatory excellence.
Work in a collaborative environment with opportunities for professional growth and skill development.
Engage with cutting-edge pharmacovigilance systems and processes in a leading life sciences company.
Equal Opportunity Employer:
Cencora provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or other protected classes. The company also provides reasonable accommodations for individuals with disabilities during the employment process.
Apply Now to join Cencora as a Medical Reviewer – Case Processing and contribute to global patient safety and pharmacovigilance excellence.
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