Medical Reviewer – Case Processing
Pharmacovigilance & Drug Safety
Location: Noida, India
Employment Type: Full-Time
Category: Consulting
Posted Date: December 17, 2025
Job ID: R2522052
Affiliated Entity: PharmaLex India Private Limited (A Cencora Company)
About Cencora
Cencora is a global healthcare services organization dedicated to advancing patient safety and improving health outcomes worldwide. With a strong presence across the pharmaceutical, biotechnology, and life sciences sectors, Cencora partners with organizations to deliver high-quality, compliant, and science-driven solutions. Our people are central to our mission of creating healthier futures for patients and communities globally.
Role Overview
Cencora is seeking a highly experienced Medical Reviewer – Case Processing to support global pharmacovigilance operations. This role is responsible for end-to-end medical review of Individual Case Safety Reports (ICSRs), ensuring clinical accuracy, regulatory compliance, and high-quality medical assessment in accordance with global pharmacovigilance standards.
The position requires strong medical judgment, advanced pharmacovigilance expertise, and the ability to mentor teams while working within complex, regulated environments.
Key Responsibilities
Perform initial medical assessment and detailed medical review of ICSRs within validated safety databases.
Review and confirm accurate selection and documentation of adverse events from source documents.
Evaluate and validate seriousness criteria, MedDRA coding, suspect and concomitant medications, medical history, laboratory data, labeling assessment, causality, and case narratives.
Provide clear, compliant Company Causality and Medical Review comments within the safety database.
Respond to medical and process-related queries raised by Case Owners during workflow review.
Identify and document follow-up information requirements not already captured in the safety system.
Ensure complete documentation of medical review activities within the medical review workflow.
Escalate complex or high-risk cases to the Team Lead or Line Manager in a timely manner.
Train and mentor pharmacovigilance associates on adverse event identification, case processing, and PV conventions.
Maintain up-to-date knowledge of product safety profiles across therapeutic areas.
Demonstrate strong understanding and application of GVP, GCP, ICH, EMA, and FDA guidelines.
Participate actively in internal project discussions, safety governance meetings, and cross-functional collaborations.
Support internal and external audits, inspections, and regulatory interactions.
Perform additional drug safety and pharmacovigilance activities as assigned by management.
Required Qualifications
Medical Degree (MBBS or equivalent) is mandatory.
Postgraduate qualification in any medical specialty is preferred but not mandatory.
Experience Requirements
Minimum 8 years of relevant experience in Pharmacovigilance and Drug Safety.
Proven hands-on experience in ICSR medical review, causality assessment, MedDRA coding oversight, and regulatory compliance.
Prior experience within pharmaceutical companies, CROs, consulting organizations, or life sciences environments is strongly preferred.
Skills and Competencies
Strong knowledge of global pharmacovigilance regulations, SOPs, and safety databases.
Excellent analytical, documentation, and organizational skills.
High level of accountability, precision, and ability to work under regulatory timelines and pressure.
Strong interpersonal and mentoring skills with a collaborative team-oriented mindset.
Professional proficiency in spoken and written English.
Service-oriented approach with experience working in structured corporate environments.
What Cencora Offers
Cencora offers a professional and inclusive work environment with opportunities to work on global projects and develop long-term careers in pharmacovigilance and drug safety. Benefits and compensation are aligned with local market practices and may vary by location and employment terms.
Equal Employment Opportunity
Cencora is committed to equal employment opportunity and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or any other legally protected characteristic. All employment-related decisions are based on business needs, job requirements, and individual qualifications.
Reasonable accommodations are provided to qualified individuals with disabilities in accordance with applicable laws.
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