Job Description

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

• As a Lead GPV Professional, Medical Reviewer within Global ICSR Operations, the role supports the medical review of individual case safety reports (ICSRs) originating from spontaneous and organized data collection.
• The position contributes to the quality and consistency of medical content in ICSRs and assists case processors with medical judgment, MedDRA coding, and causality assessments under supervision.
• Collaborates closely with senior medical reviewers and team leads to contribute to the accuracy and compliance of case documentation.

How you’ll spend your day

• Assist in the medical review and clarification of trial-related AEs and post-marketing ADRs, including narrative consistency, seriousness, expectedness, and completeness of clinical information.
• Support MedDRA coding of adverse events and contribute to causality and labeling assessments under guidance.
• Collaborate with senior reviewers to clarify medical content and ensure alignment with internal standards and regulatory expectations.
• Participate in quality checks and help identify areas for improvement in case documentation and medical consistency.
• Contribute to training sessions, workshops, and knowledge-sharing activities within the team.
• Support audit and inspection readiness by ensuring documentation and processes are compliant and well-maintained.
• Maintain awareness of evolving pharmacovigilance practices and regulatory requirements through internal learning and team discussions.

Your experience and qualifications

• Medical Degree (MBBS or equivalent) with valid license to practice.

• 1–2 years of clinical experience; prior exposure to pharmacovigilance or medical review is needed

• Strong interest in drug safety, clinical data, and regulatory science.

• Fluent in English (written and spoken).

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Job Tags

Similar Jobs