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Medical Reviewer Case Processing

Cencora
Cencora
8+ years
Not Disclosed
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Reviewer – Case Processing
Location: Noida, India | Category: Consulting | Employment Type: Full-Time | Job ID: R2522052 | Posted: December 17, 2025

About Cencora
Cencora is a global healthcare leader committed to improving the lives of people and animals worldwide. Our employees are central to our mission, driving innovative solutions and maintaining the highest standards of drug safety, compliance, and quality.

Role Overview
We are seeking an experienced Medical Reviewer to perform comprehensive medical reviews and case processing of Individual Case Safety Reports (ICSRs). This role ensures accurate safety data management, regulatory compliance, and effective mentoring of pharmacovigilance associates. The position is based in Noida, India, and offers exposure to global pharmacovigilance operations and therapeutic areas.

Key Responsibilities

  • Conduct initial assessment and full medical review of ICSRs in the safety database.

  • Verify adverse event selection, seriousness criteria, MedDRA coding, suspect drug, concomitant medications, lab data, medical history, labeling, causality assessment, and provide company causality comments.

  • Respond to queries and comments from Case Owners in the safety database.

  • Train and mentor PV associates on event capturing, PV conventions, and database processes.

  • Maintain updated knowledge of product safety profiles across therapeutic areas.

  • Escalate complex cases to Team Lead or Line Manager.

  • Document follow-up information and case comments accurately in the database.

  • Ensure compliance with GPvP, GCP, ICH, EMA, and FDA guidelines.

  • Participate actively in internal project meetings, audits, and inspections.

  • Perform other drug safety activities as assigned by management.

Qualifications & Experience

  • Medical degree required; postgraduate degree in any discipline is advantageous but not mandatory.

  • Minimum 8 years of relevant experience in pharmacovigilance and drug safety.

Skills & Competencies

  • Strong interpersonal, organizational, and team collaboration skills.

  • High sense of responsibility, dedication, and ability to perform under pressure.

  • Service-oriented mindset with experience in corporate, pharmaceutical, or life sciences environments preferred.

  • Excellent written and verbal communication skills; fluent in English.

What Cencora Offers

  • Competitive compensation and benefits aligned with local market practices.

  • Opportunities for professional development and exposure to global pharmacovigilance operations.

  • Supportive and inclusive workplace culture emphasizing safety, compliance, and innovation.

Equal Employment Opportunity
Cencora provides equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or other legally protected categories. Reasonable accommodations are available for individuals with disabilities during the employment process.

Affiliated Company: PharmaLex India Private Limited

Application Information
Interested candidates can apply through the company portal. For accommodation requests, contact hrsc@cencora.com or call 888.692.2272.