Lead GPV Professional – Medical Reviewer
Location: Bangalore, India
Company: Teva Pharmaceuticals
Job ID: 65232
Date Posted: December 5, 2025
Employment Type: Full-Time
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to making high-quality, affordable healthcare accessible to millions of patients worldwide. With operations in nearly 60 countries and products included on the WHO Essential Medicines List, Teva’s mission is to improve lives through safe, effective, and reliable therapies. More than 200 million people take a Teva medicine every day.
Position Overview
Teva is seeking a Lead GPV Professional, Medical Reviewer to join its Global ICSR Operations team. This role plays a critical part in ensuring the medical quality, accuracy, and compliance of Individual Case Safety Reports (ICSRs) from both spontaneous and organized data sources. The position supports medical judgment, MedDRA coding, causality assessment, and narrative review under the supervision of senior medical reviewers.
This is an excellent opportunity for a medically trained professional to strengthen expertise in pharmacovigilance, global drug safety regulations, and case review processes.
Key Responsibilities
Medical Review & Case Evaluation
Assist in the medical review of clinical trial AEs and post-marketing ADRs, ensuring consistency, accuracy, seriousness assessment, expectedness evaluation, and completeness of clinical information.
Support MedDRA coding of adverse events and contribute to causality and labeling assessments under guidance from senior reviewers.
Collaborate closely with senior medical reviewers and team leads to ensure medical content meets regulatory, scientific, and internal compliance standards.
Quality & Compliance
Participate in internal quality checks and support identification of improvement areas in case documentation.
Contribute to audit and inspection readiness by maintaining high standards of documentation accuracy and process compliance.
Stay updated on evolving pharmacovigilance regulations, global safety practices, and medical review methodologies.
Team Collaboration & Training
Participate in knowledge-sharing sessions, internal workshops, and training initiatives.
Provide medical clarifications to case processors and support harmonization of safety data across the organization.
Required Qualifications & Experience
Education
Medical Degree (MBBS or equivalent) with a valid license to practice.
Experience
1 to 2 years of clinical experience is required.
Prior exposure to pharmacovigilance or medical review is mandatory.
Familiarity with global drug safety regulations, ICSRs, MedDRA terminology, and clinical data interpretation is preferred.
Skills & Competencies
Strong interest in drug safety, clinical research, and regulatory science.
Ability to review clinical narratives with precision and medical accuracy.
Proficiency in English (written and spoken).
Strong analytical mindset, attention to detail, and capability to work in a structured, compliance-driven environment.
Why Join Teva
Opportunity to contribute to global patient safety and public health.
Work within a high-impact pharmacovigilance function supporting products used worldwide.
Engage with international safety experts and expand your expertise in medical review and regulatory compliance.
Equal Employment Opportunity
Teva Pharmaceuticals is committed to providing equal employment opportunities without discrimination based on age, race, religion, gender, disability, pregnancy status, national origin, veteran status, sexual orientation, or any other protected characteristic. Teva supports applicants who require reasonable accommodations during the recruitment process, ensuring a fair and inclusive hiring experience.
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