Job Title: Medical Reviewer – Case Processing
Category: Pharmacovigilance / Drug Safety
Location: Noida, India
Employment Type: Full-Time
Job ID: R2522052
Cencora is a leading global healthcare company committed to creating healthier futures for people and animals. Our teams operate at the heart of health innovation, ensuring safe and effective therapies reach patients worldwide. If you want to make a meaningful impact in drug safety and pharmacovigilance, join our team and help shape the future of healthcare.
Conduct initial assessment and medical review of Individual Case Safety Reports (ICSRs) in the safety database.
Verify adverse events against source documents, including seriousness criteria, MedDRA coding, suspect drugs, concomitant medications, lab data, and medical history.
Evaluate causality, review narratives, and provide Company Causality Comments.
Respond to queries and comments from case owners in the safety database.
Train and mentor pharmacovigilance associates on event capture and PV conventions.
Maintain up-to-date knowledge of product safety profiles across therapeutic areas.
Escalate complex case issues to the Team Lead or Line Manager.
Document case reviews and comments in the medical review workflow of the safety database.
Maintain compliance with GVP, GCP, ICH, EMA, FDA guidelines, and internal SOPs.
Actively participate in internal project meetings, audits, and inspections.
Perform additional drug safety-related tasks as assigned by management.
Degree in Medicine (MBBS); Postgraduate degree in any discipline is an advantage but not mandatory.
Minimum 8 years of relevant experience in Pharmacovigilance and Drug Safety.
Previous exposure to corporate, pharmaceutical, or life sciences environments is advantageous.
Strong interpersonal and organizational skills; ability to work collaboratively in a team.
High sense of responsibility, dedication, and ability to work under pressure.
Strong service orientation with attention to detail and accuracy.
Excellent written and spoken English communication skills.
Deep understanding of PV processes, case review, safety databases, and regulatory guidelines.
Work on global pharmacovigilance projects with exposure to international regulatory standards.
Opportunity to contribute to patient safety and healthcare outcomes worldwide.
Professional growth through training, mentoring, and exposure to complex drug safety workflows.
Inclusive work environment committed to equal employment opportunity and providing reasonable accommodations for individuals with disabilities.
Cencora provides equal employment opportunities to all applicants and employees, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other class protected by law. All hiring, promotions, compensation, and training comply with these principles.
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