Medical Reviewer – Case Processing
Location: Noida, India
Category: Consulting / Pharmacovigilance
Job Type: Full-Time
Experience Required: Minimum 8 Years
Job ID: R2522052
About Cencora
Cencora is a global leader in healthcare solutions dedicated to creating healthier futures for people and animals. We prioritize innovation, safety, and excellence in all aspects of our work. At Cencora, every team member plays a vital role in ensuring the safety and efficacy of pharmaceutical products worldwide. Join us to contribute to cutting-edge pharmacovigilance practices and global drug safety initiatives.
Position Overview
The Medical Reviewer – Case Processing will be responsible for the medical evaluation and oversight of Individual Case Safety Reports (ICSRs) in compliance with global pharmacovigilance standards. This role ensures accurate safety data, appropriate coding, and regulatory compliance, while providing guidance and mentorship to pharmacovigilance associates.
Key Responsibilities
Conduct initial assessment and medical review of ICSRs in the safety database.
Verify adverse event coding, seriousness criteria, suspect drugs, concomitant medications, lab data, and medical history.
Review narratives and provide company causality comments.
Respond to queries from Case Owners in the safety database.
Train and mentor pharmacovigilance associates on event capture and PV conventions.
Maintain current knowledge of product safety profiles across therapeutic areas.
Escalate complex case issues to the Team Lead or Line Manager.
Document review comments and follow-up actions within the safety database.
Ensure compliance with ICH, EMA, FDA guidelines, GCP, and GPvP standards.
Actively participate in internal project meetings, audits, and inspections.
Perform additional drug safety-related activities as assigned by management.
Qualifications
Medical degree (MBBS or equivalent).
Postgraduate degree in any discipline is an advantage but not mandatory.
Experience
Minimum 8 years of relevant experience in Pharmacovigilance and Drug Safety.
Prior exposure to the pharmaceutical, biotech, or life sciences industry is preferred.
Skills & Competencies
Strong interpersonal, organizational, and communication skills.
Ability to work effectively under pressure and deadlines.
High sense of responsibility and dedication.
Service-oriented mindset with a proactive approach to problem-solving.
Fluent in spoken and written English.
Why Join Cencora
Opportunity to work at the forefront of global pharmacovigilance.
Collaborate with multinational teams across therapeutic areas.
Contribute to regulatory compliance and patient safety initiatives.
Be part of a values-driven organization committed to equality, inclusion, and professional growth.
Equal Opportunity & Accessibility
Cencora provides equal employment opportunities and reasonable accommodations for individuals with disabilities during the recruitment process. We are committed to a diverse, inclusive, and harassment-free workplace.
Apply today to join Cencora and advance your career in medical review and pharmacovigilance case processing.
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